Exact Mass: 132.066065

Exact Mass Matches: 132.066065

Found 226 metabolites which its exact mass value is equals to given mass value 132.066065, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Cinnamaldehyde

Cinnamaldehyde, United States Pharmacopeia (USP) Reference Standard

C9H8O (132.0575118)


(E)-cinnamaldehyde is the E (trans) stereoisomer of cinnamaldehyde, the parent of the class of cinnamaldehydes. It has a role as a hypoglycemic agent, an EC 4.3.1.24 (phenylalanine ammonia-lyase) inhibitor, a vasodilator agent, an antifungal agent, a flavouring agent, a plant metabolite and a sensitiser. It is a 3-phenylprop-2-enal and a member of cinnamaldehydes. Cinnamaldehyde is a naturally occurring flavonoid that gives the spice cinnamon its flavour and odour. It occurs naturally in the bark of cinnamon trees and other species of the genus Cinnamomum such as camphor and cassia. Sensitivity to cinnamaldehyde may be identified with a clinical patch test. Cinnamaldehyde is a Standardized Chemical Allergen. The physiologic effect of cinnamaldehyde is by means of Increased Histamine Release, and Cell-mediated Immunity. Cinnamaldehyde is a natural product found in Chaerophyllum bulbosum, Cinnamomum sieboldii, and other organisms with data available. Cinnamaldehyde is the aldehyde that gives cinnamon its flavor and odor. Cinnamaldehyde occurs naturally in the bark of cinnamon trees and other species of the genus Cinnamomum like camphor and cassia. These trees are the natural source of cinnamon, and the essential oil of cinnamon bark is about 90\\\\% cinnamaldehyde. Cinnamaldehyde is also used as a fungicide. Proven effective on over 40 different crops, cinnamaldehyde is typically applied to the root systems of plants. Its low toxicity and well-known properties make it ideal for agriculture. To a lesser extent, cinnamaldehyde is an effective insecticide, and its scent is also known to repel animals like cats and dogs. Cinnamaldehyde is also known as a corrosion inhibitor for steel and other ferrous alloys in corrosive fluids. It can be used in combination with additional components such as dispersing agents, solvents and other surfactants. Concentrated cinnamaldehyde is a skin irritant, and the chemical is toxic in large doses, but no agencies suspect the compound is a carcinogen or poses a long-term health hazard. Most cinnamaldehyde is excreted in urine as cinnamic acid, an oxidized form of cinnamaldehyde. Cinnamaldehyde is a metabolite found in or produced by Saccharomyces cerevisiae. Cinnamaldehyde, also known as (E)-3-phenyl-2-propenal or 3-phenylacrylaldehyde, is a member of the class of compounds known as cinnamaldehydes. Cinnamaldehydes are organic aromatic compounds containing a cinnamlaldehyde moiety, consisting of a benzene and an aldehyde group to form 3-phenylprop-2-enal. Cinnamaldehyde is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Cinnamaldehyde is a sweet, candy, and cinnamon tasting compound and can be found in a number of food items such as sour cherry, rubus (blackberry, raspberry), horseradish, and sea-buckthornberry, which makes cinnamaldehyde a potential biomarker for the consumption of these food products. Cinnamaldehyde can be found primarily in feces, as well as in human neuron and skin tissues. Cinnamaldehyde exists in all eukaryotes, ranging from yeast to humans. Cinnamaldehyde is a non-carcinogenic (not listed by IARC) potentially toxic compound. Cinnamaldehyde is an organic compound with the formula C6H5CH=CHCHO. Occurring naturally as predominantly the trans (E) isomer, it gives cinnamon its flavor and odor. It is a flavonoid that is naturally synthesized by the shikimate pathway. This pale yellow, viscous liquid occurs in the bark of cinnamon trees and other species of the genus Cinnamomum. The essential oil of cinnamon bark is about 50\\\\% cinnamaldehyde . The specific symptoms that can result from cinnamic aldehyde allergy can vary considerably amongst patients from a severe anaphylactic reaction to asthma, abdominal symptoms, eczema or headaches (L2140) (T3DB). Cinnamaldehyde is the aldehyde that gives cinnamon its flavor and odor. Cinnamaldehyde occurs naturally in the bark of cinnamon trees and other species of the genus Cinnamomum like camphor and cassia. These trees are the natural source of cinnamon, and the essential oil of cinnamon bark is about 90\\\\% cinnamaldehyde. Cinnamaldehyde is also used as a fungicide. Proven effective on over 40 different crops, cinnamaldehyde is typically applied to the root systems of plants. Its low toxicity and well-known properties make it ideal for agriculture. To a lesser extent, cinnamaldehyde is an effective insecticide, and its scent is also known to repel animals like cats and dogs. Cinnamaldehyde is also known as a corrosion inhibitor for steel and other ferrous alloys in corrosive fluids. It can be used in combination with additional components such as dispersing agents, solvents and other surfactants. Concentrated cinnamaldehyde is a skin irritant, and the chemical is toxic in large doses, but no agencies suspect the compound is a carcinogen or poses a long-term health hazard. Most cinnamaldehyde is excreted in urine as cinnamic acid, an oxidized form of cinnamaldehyde. D020011 - Protective Agents > D016587 - Antimutagenic Agents D000074385 - Food Ingredients > D005503 - Food Additives D010592 - Pharmaceutic Aids > D005421 - Flavoring Agents D000970 - Antineoplastic Agents Acquisition and generation of the data is financially supported in part by CREST/JST. trans-Cinnamaldehyde can be used to prepare highly polyfunctionalized furan ring by reaction of alkyl isocyanides with dialkyl acetylenedicarboxylate[1]. trans-Cinnamaldehyde can be used to synthesize trans-cinnamaldehyde -β-cyclodextrin complex, an antimicrobial edible coating that increases the shelf life of fresh-cut fruits[2]. trans-Cinnamaldehyde can be used to prepare highly polyfunctionalized furan ring by reaction of alkyl isocyanides with dialkyl acetylenedicarboxylate[1]. trans-Cinnamaldehyde can be used to synthesize trans-cinnamaldehyde -β-cyclodextrin complex, an antimicrobial edible coating that increases the shelf life of fresh-cut fruits[2].

   
   

Indanone

2,3-dihydro-1H-inden-1-one

C9H8O (132.0575118)


Indanone is part of the Steroid hormone biosynthesis, and Arachidonic acid metabolism pathways. It is a substrate for: Aldo-keto reductase family 1 member C1, and Aldo-keto reductase family 1 member C3. D018501 - Antirheumatic Agents > D006074 - Gout Suppressants > D014528 - Uricosuric Agents D002317 - Cardiovascular Agents > D045283 - Natriuretic Agents D045283 - Natriuretic Agents > D004232 - Diuretics

   

1H-Indol-3-amine

1H-indol-3-amine

C8H8N2 (132.0687448)


   

Methylenediurea

Urea,N,N-methylenebis-

C3H8N4O2 (132.0647228)


   

Atropaldehyde

BENZENEACETALDEHYDE, .ALPHA.-METHYLENE-

C9H8O (132.0575118)


Atropaldehyde is a metabolite of felbamate. Felbamate (marketed under the brand name Felbatol by MedPointe) is an anti-epileptic drug used in the treatment of epilepsy. It is used to treat partial seizures (with and without generalization) in adults and partial and generalized seizures associated with Lennox-Gastaut syndrome in children. However, an increased risk of potentially fatal aplastic anemia and/or liver failure limit the drugs usage to severe refractory epilepsy. (Wikipedia)

   
   

4-Methylpyrrolo[1,2-a]pyrazine

4-Methylpyrrolo[1,2-a]pyrazine

C8H8N2 (132.0687448)


4-Methylpyrrolo[1,2-a]pyrazine is a component of roast beef aroma. Component of roast beef aroma

   

1-Methylpyrrolo[1,2-a]pyrazine

1-Methylpyrrolo[1,2-a]pyrazine

C8H8N2 (132.0687448)


1-Methylpyrrolo[1,2-a]pyrazine is a maillard product. Maillard product

   

4-Mercapto-4-methyl-2-pentanone

4-Sulphanyl-4-methylpentan-2-one

C6H12OS (132.0608822)


4-Mercapto-4-methyl-2-pentanone is found in alcoholic beverages. 4-Mercapto-4-methyl-2-pentanone is present in Sauvignon wine Present in Sauvignon wines. 4-Mercapto-4-methyl-2-pentanone is found in alcoholic beverages.

   

(Z)-Cinnamaldehyde

(2Z)-3-phenylprop-2-enal

C9H8O (132.0575118)


(Z)-Cinnamaldehyde is found in ceylan cinnamon. Cinnamaldehyde is the organic compound that gives cinnamon its flavor and odor. This pale yellow viscous liquid occurs naturally in the bark of cinnamon trees and other species of the genus Cinnamomum. The essential oil of cinnamon bark is about 90\\% cinnamaldehyde (Wikipedia). Cinnamaldehyde is the organic compound that gives cinnamon its flavor and odor. This pale yellow viscous liquid occurs naturally in the bark of cinnamon trees and other species of the genus Cinnamomum. The essential oil of cinnamon bark is about 90\\% cinnamaldehyde. (Z)-3-Phenyl-2-propenal is found in ceylon cinnamon.

   

2,5-Dimethyl-3-mercaptotetrahydrofuran

(Z+E)-2,5-dimethyl-3-tetrahydrofuran thiol

C6H12OS (132.0608822)


2,5-Dimethyl-3-mercaptotetrahydrofuran is used as a food additive [EAFUS] ("EAFUS: Everything Added to Food in the United States. [http://www.eafus.com/]")

   

4-(Methylthio)-2-pentanone

4-(Methylsulphanyl)pentan-2-one

C6H12OS (132.0608822)


4-(Methylthio)-2-pentanone is used as a food additive [EAFUS] ("EAFUS: Everything Added to Food in the United States. [http://www.eafus.com/]")

   

3-Mercapto-2-methylpentanal

2-Methyl-3-sulphanylpentanal

C6H12OS (132.0608822)


Aroma constituent of cut raw onion. 3-Mercapto-2-methylpentanal is found in onion-family vegetables. 3-Mercapto-2-methylpentanal is found in onion-family vegetables. Aroma constituent of cut raw onio

   

S-Methyl 3-methylthiobutyrate

Butanethioic acid, 3-methyl-, S-methyl ester

C6H12OS (132.0608822)


S-Methyl 3-methylthiobutyrate is found in fruits. S-Methyl 3-methylthiobutyrate is produced by micrococaceae and coryneform bacteria isolated from cheeses. Also in hop oil, honeydew melon, galbanum oil and (tentatively) cantaloupes. S-Methyl 3-methylthiobutyrate is a flavouring ingredient. Production by micrococaceae and coryneform bacteria isolated from cheesesand is) also in hop oil, honeydew melon, galbanum oil and (tentatively) cantaloupes. Flavouring ingredient. S-Methyl 3-methylthiobutyrate is found in milk and milk products and fruits.

   

2-Methylcumarone

2-methyl-1-benzofuran

C9H8O (132.0575118)


2-Methylcumarone belongs to the family of Benzofurans. These are organic compounds containing a benzene ring fused to a furan

   

Acrylophenone

1-phenylprop-2-en-1-one

C9H8O (132.0575118)


   

1H-Indol-2-amine

1H-indol-2-amine

C8H8N2 (132.0687448)


   

2-Methylbenzimidazole

2-Methyl-1H-benzo[d]imidazole

C8H8N2 (132.0687448)


   

3-Phenylprop-2-enal

3-Phenylacrylaldehyde

C9H8O (132.0575118)


   

2H-Chromene

5,7-Dimethoxy-2-methyl-2H-benzopyran

C9H8O (132.0575118)


   

4-Aminoindole

1H-indol-4-amine

C8H8N2 (132.0687448)


   

4H-1-Benzopyran

4H-1-Benzopyran

C9H8O (132.0575118)


   

5-Aminoindole

1H-indol-5-amine

C8H8N2 (132.0687448)


   

1-Methylthiopentan-3-one

1-(methylsulfanyl)pentan-3-one

C6H12OS (132.0608822)


1-methylthiopentan-3-one is a member of the class of compounds known as ketones. Ketones are organic compounds in which a carbonyl group is bonded to two carbon atoms R2C=O (neither R may be a hydrogen atom). Ketones that have one or more alpha-hydrogen atoms undergo keto-enol tautomerization, the tautomer being an enol. 1-methylthiopentan-3-one is slightly soluble (in water) and an extremely weak acidic compound (based on its pKa). 1-methylthiopentan-3-one can be found in kohlrabi, which makes 1-methylthiopentan-3-one a potential biomarker for the consumption of this food product.

   

3-mercapto-4-methyl-2-pentanone

4-Methyl-3-sulphanylpentan-2-one

C6H12OS (132.0608822)


Flavouring compound [Flavornet]

   

5-methyl-5(H)-cyclopentapyrazine

5-Methyl-5H-cyclopenta[b]pyrazine

C8H8N2 (132.0687448)


Flavouring compound [Flavornet]

   

4-Aminoindole

4-Aminoindole

C8H8N2 (132.0687448)


KEIO_ID A035

   

5-Aminoindole

5-Aminoindole

C8H8N2 (132.0687448)


KEIO_ID A036

   

4,6,8-nonatriyn-1-ol|nona-4,6,8-triyn-1-ol|Nona-4.6.8-triin-1-ol|Nonatriin-(4.6.8)-ol-(1)

4,6,8-nonatriyn-1-ol|nona-4,6,8-triyn-1-ol|Nona-4.6.8-triin-1-ol|Nonatriin-(4.6.8)-ol-(1)

C9H8O (132.0575118)


   

(+)Nona-3,4-dien-6,8-diin-1-ol|(+-)-marasin|(+/-)-marasin|(-)-marasin|(-)-Nona-3,4-dien-6,8-diin-1-ol|(R)-3,4-Nonadiene-6,8-diyn-1-ol|(R)-Nona-3,4-dien-6,8-diin-1-ol|(R)-nona-3,4-diene-6,8-diyn-1-ol|(Ra)-nona-3,4-diene-6,8-diyn-1-ol|(S)-3,4-Nonadiene-6,8-diyn-1-ol|marasin|nona-3,4-diene-6,8-diyn-1-ol|Nonadien-(3.4)-diin-(6.8)-ol-(1), DL-Marasin|R-(-)-Marasin

(+)Nona-3,4-dien-6,8-diin-1-ol|(+-)-marasin|(+/-)-marasin|(-)-marasin|(-)-Nona-3,4-dien-6,8-diin-1-ol|(R)-3,4-Nonadiene-6,8-diyn-1-ol|(R)-Nona-3,4-dien-6,8-diin-1-ol|(R)-nona-3,4-diene-6,8-diyn-1-ol|(Ra)-nona-3,4-diene-6,8-diyn-1-ol|(S)-3,4-Nonadiene-6,8-diyn-1-ol|marasin|nona-3,4-diene-6,8-diyn-1-ol|Nonadien-(3.4)-diin-(6.8)-ol-(1), DL-Marasin|R-(-)-Marasin

C9H8O (132.0575118)


   

Malonic acid dihydrazide

Malonic acid dihydrazide

C3H8N4O2 (132.0647228)


   
   

3,5,7-Nonatriyn-1-ol|nona-3,5,7-triyn-1-ol|Nona-3.5.7-triin-1-ol

3,5,7-Nonatriyn-1-ol|nona-3,5,7-triyn-1-ol|Nona-3.5.7-triin-1-ol

C9H8O (132.0575118)


   

3-Methylpyrrolo[1,2-a]pyrazine

3-Methylpyrrolo[1,2-a]pyrazine

C8H8N2 (132.0687448)


A pyrrolopyrazine that is pyrrolo[1,2-a]pyrazine in which the hydrogen at position 3 is replaced by a methyl group.

   
   

1H-inden-5-ol

1H-inden-5-ol

C9H8O (132.0575118)


   

trans-cinnamaldehyde

trans-cinnamaldehyde

C9H8O (132.0575118)


trans-Cinnamaldehyde can be used to prepare highly polyfunctionalized furan ring by reaction of alkyl isocyanides with dialkyl acetylenedicarboxylate[1]. trans-Cinnamaldehyde can be used to synthesize trans-cinnamaldehyde -β-cyclodextrin complex, an antimicrobial edible coating that increases the shelf life of fresh-cut fruits[2]. trans-Cinnamaldehyde can be used to prepare highly polyfunctionalized furan ring by reaction of alkyl isocyanides with dialkyl acetylenedicarboxylate[1]. trans-Cinnamaldehyde can be used to synthesize trans-cinnamaldehyde -β-cyclodextrin complex, an antimicrobial edible coating that increases the shelf life of fresh-cut fruits[2].

   

Cinnamaldehyde

trans-cinnamaldehyde

C9H8O (132.0575118)


Cinnamaldehyde is the organic compound that gives cinnamon its flavor and odor. This pale yellow viscous liquid occurs naturally in the bark of cinnamon trees and other species of the genus Cinnamomum. The essential oil of cinnamon bark is about 90\\% cinnamaldehyde. 3-Phenyl-2-propenal is found in many foods, some of which are fig, cloves, anise, and wild celery.

   

(Z)-Cinnamaldehyde

(Z)-Cinnamaldehyde

C9H8O (132.0575118)


   

4-Methyl-4-thiolpentan-2-one

4-Sulphanyl-4-methylpentan-2-one

C6H12OS (132.0608822)


   

cis-Cinnamaldehyde

(2Z)-3-phenylprop-2-enal

C9H8O (132.0575118)


   

2,5-dimethyloxolane-3-thiol

(Z+E)-2,5-dimethyl-3-tetrahydrofuran thiol

C6H12OS (132.0608822)


   

4-(Methylthio)-2-pentanone

4-(methylsulfanyl)pentan-2-one

C6H12OS (132.0608822)


   

1-Methylpyrrolo[1,2-a]pyrazine

1-Methylpyrrolo[1,2-a]pyrazine

C8H8N2 (132.0687448)


   

4-Methylpyrrolo[1,2-a]pyrazine

4-Methylpyrrolo[1,2-a]pyrazine

C8H8N2 (132.0687448)


   

3-Mercapto-2-methylpentanal

3-Mercapto-2-methylpentanal

C6H12OS (132.0608822)


   

FEMA 3864

Butanethioic acid, 3-methyl-, S-methyl ester

C6H12OS (132.0608822)


   

FOH 9:6

3,4(R)-octadien-5,7-diyn-1-ol

C9H8O (132.0575118)


   

Marasin

3,4-nonadiene-6,8-diyn-1-ol

C9H8O (132.0575118)


   

4-Mercapto-4-methylpentan-2-one

4-Mercapto-4-methylpentan-2-one

C6H12OS (132.0608822)


An alkylthiol that is 4-methylpentan-2-one substituted at position 4 by a mercapto group.

   

1H-indol-7-amine

1H-indol-7-amine

C8H8N2 (132.0687448)


   

Methyl trans-3-fluorocyclobutanecarboxylate

Methyl trans-3-fluorocyclobutanecarboxylate

C6H9FO2 (132.0586546)


   

4-methyl-1H-pyrrolo[2,3-c]pyridine

4-methyl-1H-pyrrolo[2,3-c]pyridine

C8H8N2 (132.0687448)


   

6H-Pyrrolo[3,2-b]pyridine,2-methyl-(9CI)

6H-Pyrrolo[3,2-b]pyridine,2-methyl-(9CI)

C8H8N2 (132.0687448)


   
   

methylvinyldimethoxysilane

methylvinyldimethoxysilane

C5H12O2Si (132.0606532)


   

Malonic dihydrazide

Malonic dihydrazide

C3H8N4O2 (132.0647228)


   

4-Cyanobenzylamine

4-Cyanobenzylamine

C8H8N2 (132.0687448)


   

2,6-Dimethylpyridine-4-carbonitrile

2,6-Dimethylpyridine-4-carbonitrile

C8H8N2 (132.0687448)


   

PROPYLVINYLETHER

PROPYLVINYLETHER

C6H9FO2 (132.0586546)


   

5-methylimidazo[1,5-a]pyridine

5-methylimidazo[1,5-a]pyridine

C8H8N2 (132.0687448)


   

2-amino-5-methylbenzonitril

2-amino-5-methylbenzonitril

C8H8N2 (132.0687448)


   

1-Methylbenzimidazole

1-Methylbenzimidazole

C8H8N2 (132.0687448)


   

2-Methyl-4-azaindole

2-Methyl-4-azaindole

C8H8N2 (132.0687448)


   

2-Amino-6-methylbenzonitrile

2-Amino-6-methylbenzonitrile

C8H8N2 (132.0687448)


   

1H-Indol-6-amine

1H-Indol-6-amine

C8H8N2 (132.0687448)


   

2,2-Bipyrrole

2,2-Bipyrrole

C8H8N2 (132.0687448)


   

CYCLOHEPTYL CHLORIDE

CYCLOHEPTYL CHLORIDE

C7H13Cl (132.0705728)


   

6-Methyl-5-azaindole

6-Methyl-5-azaindole

C8H8N2 (132.0687448)


   
   

(2S,4S)-4-FLUOROPYRROLIDINE-2-CARBOXAMIDE

(2S,4S)-4-FLUOROPYRROLIDINE-2-CARBOXAMIDE

C5H9FN2O (132.0698876)


   

(2S,4R)-4-Fluoropyrrolidine-2-carboxamide

(2S,4R)-4-Fluoropyrrolidine-2-carboxamide

C5H9FN2O (132.0698876)


   

4-Fluoropyrrolidine-2-carboxamide

4-Fluoropyrrolidine-2-carboxamide

C5H9FN2O (132.0698876)


   

4-Ethynylanisole

1-Ethynyl-4-methoxybenzene

C9H8O (132.0575118)


   

2,5-DIMETHYLISONICOTINONITRILE

2,5-DIMETHYLISONICOTINONITRILE

C8H8N2 (132.0687448)


   

2-Cyclopentylethylchloride

2-Cyclopentylethylchloride

C7H13Cl (132.0705728)


   

3-ethylpyridine-4-carbonitrile

3-ethylpyridine-4-carbonitrile

C8H8N2 (132.0687448)


   

5-Methyl-5H-pyrrolo[2,3-b]pyridine

5-Methyl-5H-pyrrolo[2,3-b]pyridine

C8H8N2 (132.0687448)


   

4-Methyl-1-benzofuran

4-Methyl-1-benzofuran

C9H8O (132.0575118)


   

3-Amino-1H-isoindole

3-Amino-1H-isoindole

C8H8N2 (132.0687448)


   

4-FLUOROTETRAHYDRO-2H-PYRAN-4-CARBALDEHYDE

4-FLUOROTETRAHYDRO-2H-PYRAN-4-CARBALDEHYDE

C6H9FO2 (132.0586546)


   

4-(Methylamino)benzonitrile

4-(Methylamino)benzonitrile

C8H8N2 (132.0687448)


   

3-Methyl-1H-indazole

3-Methyl-1H-indazole

C8H8N2 (132.0687448)


   

2-(6-methylpyridin-3-yl)acetonitrile

2-(6-methylpyridin-3-yl)acetonitrile

C8H8N2 (132.0687448)


   

(2-Ethynylphenyl)methanol

(2-Ethynylphenyl)methanol

C9H8O (132.0575118)


   

5-Methylimidazo[1,2-a]pyridine

5-Methylimidazo[1,2-a]pyridine

C8H8N2 (132.0687448)


   

Imidazo[1,2-a]pyridine,8-methyl-

Imidazo[1,2-a]pyridine,8-methyl-

C8H8N2 (132.0687448)


   
   

3-Methyl-1H-pyrrolo[2,3-b]pyridine

3-Methyl-1H-pyrrolo[2,3-b]pyridine

C8H8N2 (132.0687448)


   

4-Vinylbenzaldehyde

4-Vinylbenzaldehyde

C9H8O (132.0575118)


   

TRANS-4-MERCAPTOCYCLOHEXANOL

TRANS-4-MERCAPTOCYCLOHEXANOL

C6H12OS (132.0608822)


   

4-Ethynyl-3-methylphenol

4-Ethynyl-3-methylphenol

C9H8O (132.0575118)


   

1-Methyl-1H-pyrrolo[2,3-b]pyridine

1-Methyl-1H-pyrrolo[2,3-b]pyridine

C8H8N2 (132.0687448)


   

5-Methyl-1H-pyrrolo[2,3-c]pyridine

5-Methyl-1H-pyrrolo[2,3-c]pyridine

C8H8N2 (132.0687448)


   

5-Methyl-1H-indazole

5-Methyl-1H-indazole

C8H8N2 (132.0687448)


   

Indene oxide

Indene oxide

C9H8O (132.0575118)


   

5-methylbenzimidazole

5-methylbenzimidazole

C8H8N2 (132.0687448)


   

2-Methyl-7-azaindole

2-Methyl-7-azaindole

C8H8N2 (132.0687448)


   

1-methyl-1H-pyrrolo[2,3-c]pyridine

1-methyl-1H-pyrrolo[2,3-c]pyridine

C8H8N2 (132.0687448)


   

5-Methyl-7-azaindole

5-Methyl-7-azaindole

C8H8N2 (132.0687448)


   

p-Aminobenzyl cyanide

p-Aminobenzyl cyanide

C8H8N2 (132.0687448)


   

2-(2-methylpyridin-4-yl)acetonitrile

2-(2-methylpyridin-4-yl)acetonitrile

C8H8N2 (132.0687448)


   

3-Methyl-1H-pyrrolo[3,2-c]pyridine

3-Methyl-1H-pyrrolo[3,2-c]pyridine

C8H8N2 (132.0687448)


   

7-methylimidazo[1,2-a]pyridine

7-methylimidazo[1,2-a]pyridine

C8H8N2 (132.0687448)


   

1-Phenyl-2-propyn-1-ol

1-Phenyl-2-propyn-1-ol

C9H8O (132.0575118)


   

5-METHYL-1H-PYRROLO[3,2-B]PYRIDINE

5-METHYL-1H-PYRROLO[3,2-B]PYRIDINE

C8H8N2 (132.0687448)


   

1-METHYL-IMIDAZO[1,5-A]PYRIDINE

1-METHYL-IMIDAZO[1,5-A]PYRIDINE

C8H8N2 (132.0687448)


   
   

4-amino-2-methylbenzonitrile

4-amino-2-methylbenzonitrile

C8H8N2 (132.0687448)


   

4,6-DIMETHYLNICOTINONITRILE

4,6-DIMETHYLNICOTINONITRILE

C8H8N2 (132.0687448)


   

4-Methyl-1H-indazole

4-Methyl-1H-indazole

C8H8N2 (132.0687448)


   

3-Mercaptopropionic acid isopropyl ester

3-Mercaptopropionic acid isopropyl ester

C6H12OS (132.0608822)


   

Propanediimidamide,N1,N3-dihydroxy-

Propanediimidamide,N1,N3-dihydroxy-

C3H8N4O2 (132.0647228)


   

indol-1-amine

indol-1-amine

C8H8N2 (132.0687448)


   

S-Methyl 2-methylthiobutyrate

S-Methyl 2-methylthiobutyrate

C6H12OS (132.0608822)


   

Pyrimidine, 5-ethynyl-2,4-dimethyl- (9CI)

Pyrimidine, 5-ethynyl-2,4-dimethyl- (9CI)

C8H8N2 (132.0687448)


   

n-Propyl 3-mercaptopropionate

n-Propyl 3-mercaptopropionate

C6H12OS (132.0608822)


   

Cyclohexane,1-chloro-1-methyl-

Cyclohexane,1-chloro-1-methyl-

C7H13Cl (132.0705728)


   

3,5-Dimethyl-2-pyridinecarbonitrile

3,5-Dimethyl-2-pyridinecarbonitrile

C8H8N2 (132.0687448)


   

3,6-Dimethyl-2-pyridinecarbonitrile

3,6-Dimethyl-2-pyridinecarbonitrile

C8H8N2 (132.0687448)


   

2-Cyano-3-ethylpyridine

2-Cyano-3-ethylpyridine

C8H8N2 (132.0687448)


   

(TETRAHYDRO-2H-THIOPYRAN-4-YL)METHANOL

(TETRAHYDRO-2H-THIOPYRAN-4-YL)METHANOL

C6H12OS (132.0608822)


   

4-Pyridinepropanenitrile

4-Pyridinepropanenitrile

C8H8N2 (132.0687448)


   

6-Methyl-7-azaindole

6-Methyl-7-azaindole

C8H8N2 (132.0687448)


   

3,5-DIMETHYLISONICOTINONITRILE

3,5-DIMETHYLISONICOTINONITRILE

C8H8N2 (132.0687448)


   

2-Amino-3-methylbenzonitrile

2-Amino-3-methylbenzonitrile

C8H8N2 (132.0687448)


   

(3-ethynylphenyl)hydrazine

(3-ethynylphenyl)hydrazine

C8H8N2 (132.0687448)


   

(4-Ethynylphenyl)methanol

(4-Ethynylphenyl)methanol

C9H8O (132.0575118)


   

1-Hydroxymethylbenzocyclobutene

1-Hydroxymethylbenzocyclobutene

C9H8O (132.0575118)


   

1,3-Bi-1H-pyrrole(9CI)

1,3-Bi-1H-pyrrole(9CI)

C8H8N2 (132.0687448)


   

2-Fluoroethyl methacrylate

2-Fluoroethyl methacrylate

C6H9FO2 (132.0586546)


   

3-Amino-p-tolunitrile

3-Amino-p-tolunitrile

C8H8N2 (132.0687448)


   

5,6-Dimethyl-2-pyridinecarbonitrile

5,6-Dimethyl-2-pyridinecarbonitrile

C8H8N2 (132.0687448)


   

7-Methyl-1H-pyrrolo[2,3-c]pyridine

7-Methyl-1H-pyrrolo[2,3-c]pyridine

C8H8N2 (132.0687448)


   

7-Methyl-1H-pyrrolo[3,2-b]pyridine

7-Methyl-1H-pyrrolo[3,2-b]pyridine

C8H8N2 (132.0687448)


   

1-chloro-4-methylcyclohexane

1-chloro-4-methylcyclohexane

C7H13Cl (132.0705728)


   

6-methylbenzofuran

6-methylbenzofuran

C9H8O (132.0575118)


   

2-ethylisonicotinonitrile

2-ethylisonicotinonitrile

C8H8N2 (132.0687448)


   

2-Amino-4-methylbenzonitrile

2-Amino-4-methylbenzonitrile

C8H8N2 (132.0687448)


   

7-Chloro-1-heptene

7-Chloro-1-heptene

C7H13Cl (132.0705728)


   

3-VINYLBENZALDEHYDE

3-VINYLBENZALDEHYDE

C9H8O (132.0575118)


   

7-Hydroxyindene

7-Hydroxyindene

C9H8O (132.0575118)


   

2-amino-2-phenylacetonitrile

2-amino-2-phenylacetonitrile

C8H8N2 (132.0687448)


   

Ethanethioic acid,S-butyl ester

Ethanethioic acid,S-butyl ester

C6H12OS (132.0608822)


   

2-methoxyphenylacetylene

2-methoxyphenylacetylene

C9H8O (132.0575118)


   

(Chloromethyl)cyclohexane

(Chloromethyl)cyclohexane

C7H13Cl (132.0705728)


   

(R)-1-N-BOC-PIPECOLAMIDE

(R)-1-N-BOC-PIPECOLAMIDE

C9H8O (132.0575118)


   

Anilinoacetonitrile

Anilinoacetonitrile

C8H8N2 (132.0687448)


   

3-(3-Pyridinyl)propanenitrile

3-(3-Pyridinyl)propanenitrile

C8H8N2 (132.0687448)


   

4-Amino-3-methylbenzonitrile

4-Amino-3-methylbenzonitrile

C8H8N2 (132.0687448)


   

2,2-DIMETHYLTHIOBUTYRIC ACID

2,2-DIMETHYLTHIOBUTYRIC ACID

C6H12OS (132.0608822)


   

phenyl 2-propynyl ether

phenyl 2-propynyl ether

C9H8O (132.0575118)


   

1-Ethynyl-3-methoxybenzene

1-Ethynyl-3-methoxybenzene

C9H8O (132.0575118)


   

3-(methylamino)benzonitrile

3-(methylamino)benzonitrile

C8H8N2 (132.0687448)


   

(s)-1-octen-3-ol

(s)-1-octen-3-ol

C9H8O (132.0575118)


   

Trimethylsilyl acetate

Trimethylsilyl acetate

C5H12O2Si (132.0606532)


   

2-Methyl-1H-pyrrolo[2,3-c]pyridine

2-Methyl-1H-pyrrolo[2,3-c]pyridine

C8H8N2 (132.0687448)


   

Pyrimidine, 2-ethynyl-4,6-dimethyl- (9CI)

Pyrimidine, 2-ethynyl-4,6-dimethyl- (9CI)

C8H8N2 (132.0687448)


   

phenyl propargyl ether

phenyl propargyl ether

C9H8O (132.0575118)


   

2-Cyanoethylpyridine

2-Cyanoethylpyridine

C8H8N2 (132.0687448)


   

s-tert-butyl thioacetate

s-tert-butyl thioacetate

C6H12OS (132.0608822)


   

4-Methyl-1H-pyrrolo[3,2-c]pyridine

4-Methyl-1H-pyrrolo[3,2-c]pyridine

C8H8N2 (132.0687448)


   

4,6-Dimethyl-2-pyridinecarbonitrile

4,6-Dimethyl-2-pyridinecarbonitrile

C8H8N2 (132.0687448)


   

3-Methyl-1H-pyrrolo[3,2-b]pyridine

3-Methyl-1H-pyrrolo[3,2-b]pyridine

C8H8N2 (132.0687448)


   

3-methyl-1H-pyrrolo[2,3-c]pyridine

3-methyl-1H-pyrrolo[2,3-c]pyridine

C8H8N2 (132.0687448)


   

6-ethylpyridine-3-carbonitrile

6-ethylpyridine-3-carbonitrile

C8H8N2 (132.0687448)


   

6-Methyl-1H-pyrrolo[3,2-b]pyridine

6-Methyl-1H-pyrrolo[3,2-b]pyridine

C8H8N2 (132.0687448)


   

1H-imidazo[1,2-a]azepine

1H-imidazo[1,2-a]azepine

C8H8N2 (132.0687448)


   

Allyl(dimethoxy)silane

Allyl(dimethoxy)silane

C5H12O2Si (132.0606532)


   

4-Aminophenylacetonitrile

2-(4-Aminophenyl)acetonitrile

C8H8N2 (132.0687448)


   

3-(Ethylsulfanyl)butanal

3-(Ethylsulfanyl)butanal

C6H12OS (132.0608822)


   

3-(Aminomethyl)benzonitrile

3-(Aminomethyl)benzonitrile

C8H8N2 (132.0687448)


   

(2-Methyl-3-pyridinyl)acetonitrile

(2-Methyl-3-pyridinyl)acetonitrile

C8H8N2 (132.0687448)


   

4-Methyl-1H-pyrrolo[2,3-b]pyridine

4-Methyl-1H-pyrrolo[2,3-b]pyridine

C8H8N2 (132.0687448)


   

5-Methylbenzofuran

5-Methylbenzofuran

C9H8O (132.0575118)


   

2-Methyl-1H-pyrrolo[3,2-c]pyridine

2-Methyl-1H-pyrrolo[3,2-c]pyridine

C8H8N2 (132.0687448)


   

7-Methyl-1H-indazole

7-Methyl-1H-indazole

C8H8N2 (132.0687448)


   

5-Amino-2-methylbenzonitrile

5-Amino-2-methylbenzonitrile

C8H8N2 (132.0687448)


   

4-Hydroxymethylbenzocyclobutene

4-Hydroxymethylbenzocyclobutene

C9H8O (132.0575118)


   

6-Methylimidazo[1,2-a]pyridine

6-Methylimidazo[1,2-a]pyridine

C8H8N2 (132.0687448)


   

2-Methylindazole

2-Methylindazole

C8H8N2 (132.0687448)


   

3-Phenyl-2-propyn-1-ol

3-Phenyl-2-propyn-1-ol

C9H8O (132.0575118)


   

2-(Aminomethyl)benzonitrile

2-(Aminomethyl)benzonitrile

C8H8N2 (132.0687448)


   

3-acetyl-4,4,5,5-tetradeuteriooxolan-2-one

3-acetyl-4,4,5,5-tetradeuteriooxolan-2-one

C6H4D4O3 (132.072450512)


   

1H-Indazole,1-methyl-

1H-Indazole,1-methyl-

C8H8N2 (132.0687448)


   

O-Ethyl butanethioate

O-Ethyl butanethioate

C6H12OS (132.0608822)


   

2-Methylimidazo(1,2-a)pyridine

2-Methylimidazo(1,2-a)pyridine

C8H8N2 (132.0687448)


   

2-(3-Aminophenyl)acetonitrile

2-(3-Aminophenyl)acetonitrile

C8H8N2 (132.0687448)


   

6-Methyl-1H-indazole

6-Methyl-1H-indazole

C8H8N2 (132.0687448)


   

Benzonitrile,2-(methylamino)-

Benzonitrile,2-(methylamino)-

C8H8N2 (132.0687448)


   

4-methyl-1H-benzimidazole

4-methyl-1H-benzimidazole

C8H8N2 (132.0687448)


   

5-Methoxy-1H-pyrrolo[2,3-c]pyridine

5-Methoxy-1H-pyrrolo[2,3-c]pyridine

C8H8N2 (132.0687448)


   

1-(Methylthio)-3-pentanone

1-(Methylthio)-3-pentanone

C6H12OS (132.0608822)


   

1H-isochromene

1H-isochromene

C9H8O (132.0575118)


   

Dihydroquinazoline

Dihydroquinazoline

C8H8N2 (132.0687448)


   

1,5-Oxathiocane

1,5-Oxathiocane

C6H12OS (132.0608822)


   

7-Methylpyrazolo[1,5-a]pyridine

7-Methylpyrazolo[1,5-a]pyridine

C8H8N2 (132.0687448)


   
   

57194-69-1

(Z)-3-phenylprop-2-enal

C9H8O (132.0575118)


   

Cinnamal

InChI=1\C9H8O\c10-8-4-7-9-5-2-1-3-6-9\h1-8H\b7-4

C9H8O (132.0575118)


D020011 - Protective Agents > D016587 - Antimutagenic Agents D000074385 - Food Ingredients > D005503 - Food Additives D010592 - Pharmaceutic Aids > D005421 - Flavoring Agents D000970 - Antineoplastic Agents trans-Cinnamaldehyde can be used to prepare highly polyfunctionalized furan ring by reaction of alkyl isocyanides with dialkyl acetylenedicarboxylate[1]. trans-Cinnamaldehyde can be used to synthesize trans-cinnamaldehyde -β-cyclodextrin complex, an antimicrobial edible coating that increases the shelf life of fresh-cut fruits[2]. trans-Cinnamaldehyde can be used to prepare highly polyfunctionalized furan ring by reaction of alkyl isocyanides with dialkyl acetylenedicarboxylate[1]. trans-Cinnamaldehyde can be used to synthesize trans-cinnamaldehyde -β-cyclodextrin complex, an antimicrobial edible coating that increases the shelf life of fresh-cut fruits[2].

   

AI3-11240

InChI=1\C9H8O\c1-7-6-8-4-2-3-5-9(8)10-7\h2-6H,1H

C9H8O (132.0575118)


   

Acrylophenone

4-07-00-00995 (Beilstein Handbook Reference)

C9H8O (132.0575118)


   

N-hydroxy-L-valinate

N-hydroxy-L-valinate

C5H10NO3- (132.066065)


A monocarboxylic acid anion, obtained by removal of a proton from the carboxylic acid group of N-hydroxy-L-valine.

   

5-Ammoniolevulinic acid

5-Ammoniolevulinic acid

C5H10NO3+ (132.066065)


A primary ammonium ion obtained by protonation of the amino group of 5-aminolevulinic acid.

   

3H-isochromene

3H-isochromene

C9H8O (132.0575118)


   

1-Indanone

1-Indanone

C9H8O (132.0575118)


D018501 - Antirheumatic Agents > D006074 - Gout Suppressants > D014528 - Uricosuric Agents D002317 - Cardiovascular Agents > D045283 - Natriuretic Agents D045283 - Natriuretic Agents > D004232 - Diuretics

   

1H-indol-3-amine

1H-indol-3-amine

C8H8N2 (132.0687448)


   

S-Methyl 3-methylbutanethioate

S-Methyl 3-methylbutanethioate

C6H12OS (132.0608822)


   

2-Methylbenzofuran

2-Methylbenzofuran

C9H8O (132.0575118)


   

2-Methylbenzimidazole

2-Methyl-1H-benzo[d]imidazole

C8H8N2 (132.0687448)


   

(Z)-3-Phenyl-2-propenal

(Z)-3-Phenyl-2-propenal

C9H8O (132.0575118)


A 3-phenylprop-2-enal that has Z configuration.

   

2H-chromene

2H-chromene

C9H8O (132.0575118)


   

Atropaldehyde

BENZENEACETALDEHYDE, .ALPHA.-METHYLENE-

C9H8O (132.0575118)


   

2,5-Dimethyltetrahydrofuran-3-thiol

(Z+E)-2,5-dimethyl-3-tetrahydrofuran thiol

C6H12OS (132.0608822)


   

1H-indol-2-amine

1H-indol-2-amine

C8H8N2 (132.0687448)


   

4H-1-Benzopyran

4H-1-Benzopyran

C9H8O (132.0575118)


   

indan-2-one

indan-2-one

C9H8O (132.0575118)


An indanone with an oxo substituent at position 2. It is a metabolite of indane.

   

(E)-Cinnamaldehyde

(E)-Cinnamaldehyde

C9H8O (132.0575118)


The E (trans) stereoisomer of cinnamaldehyde, the parent of the class of cinnamaldehydes.

   

1-phenyl-2-propyn-1-ol

NA

C9H8O (132.0575118)


{"Ingredient_id": "HBIN002980","Ingredient_name": "1-phenyl-2-propyn-1-ol","Alias": "NA","Ingredient_formula": "C9H8O","Ingredient_Smile": "C#CC(C1=CC=CC=C1)O","Ingredient_weight": "132.16 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "35261","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "20155","DrugBank_id": "NA"}

   

benzopyran Ⅱ

NA

C9H8O (132.0575118)


{"Ingredient_id": "HBIN017803","Ingredient_name": "benzopyran \u2161","Alias": "NA","Ingredient_formula": "C9H8O","Ingredient_Smile": "C1C=CC2=CC=CC=C2O1","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "36782","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

3-chlorohept-1-ene

3-chlorohept-1-ene

C7H13Cl (132.0705728)


   

n-[(2s)-butan-2-yl]carbamimidothioic acid

n-[(2s)-butan-2-yl]carbamimidothioic acid

C5H12N2S (132.07211519999998)


   

nona-3,4-dien-6,8-diyn-1-ol

nona-3,4-dien-6,8-diyn-1-ol

C9H8O (132.0575118)


   

n-(sec-butyl)carbamimidothioic acid

n-(sec-butyl)carbamimidothioic acid

C5H12N2S (132.07211519999998)