Chemical Formula: C9H7N

Chemical Formula C9H7N

Found 23 metabolite its formula value is C9H7N

Isoquinoline

Isoquinoline conjugate acid

C9H7N (129.0578462)


Isoquinoline is a flavouring agent Being an analog of pyridine, isoquinoline is a weak base, with a pKb of 8.6. It protonates to form salts upon treatment with strong acids, such as HCl. It forms adducts with Lewis acids, such as BF3. Isoquinoline is a colorless hygroscopic liquid at room temperature with a penetrating, unpleasant odor. Impure samples can appear brownish, as is typical for nitrogen heterocycles. It crystallizes platelets that have a low solubility in water but dissolve well in ethanol, acetone, diethyl ether, carbon disulfide, and other common organic solvents. It is also soluble in dilute acids as the protonated derivative. Isoquinoline is a heterocyclic aromatic organic compound. It is a structural isomer of quinoline. Isoquinoline and quinoline are benzopyridines, which are composed of a benzene ring fused to a pyridine ring. In a broader sense, the term isoquinoline is used to make reference to isoquinoline derivatives. 1-Benzylisoquinoline is the structural backbone in naturally occurring alkaloids including papaverine and morphine. The isoquinoline ring in these natural compound derives from the aromatic amino acid tyrosine Flavouring agent KEIO_ID I067

   

Quinoline

Quinoline Hydrochloride

C9H7N (129.0578462)


Quinoline is an alkaloid from various plant species including Mentha species. Also present in cocoa, black tea and scotch whiskey. Quinoline is a flavouring ingredient Quinoline is a heterocyclic aromatic organic compound. It has the formula C9H7N and is a colourless hygroscopic liquid with a strong odour. Aged samples, if exposed to light, become yellow and later brown. Quinoline is only slightly soluble in cold water but dissolves readily in hot water and most organic solvents. Quinoline is found in alcoholic beverages. Quinoline is mainly used as a building block to other specialty chemicals. Approximately 4 tonnes are produced annually according to a report published in 2005.[citation needed] Its principal use is as a precursor to 8-hydroxyquinoline, which is a versatile chelating agent and precursor to pesticides. Its 2- and 4-methyl derivatives are precursors to cyanine dyes. Oxidation of quinoline affords quinolinic acid (pyridine-2,3-dicarboxylic acid), a precursor to the herbicide sold under the name "Assert" Alkaloid from various plant subspecies including Mentha subspeciesand is also present in cocoa, black tea and scotch whiskey. Flavouring ingredient CONFIDENCE standard compound; INTERNAL_ID 2526 KEIO_ID Q008

   

3-Methylene-indolenine

3-Methyleneindolenine, conjugate acid

C9H7N (129.0578462)


3-Methylene-indolenine is an electrophilic molecule produced by the action of cytochrome P450 2F1 on 3-methylindole (3MI). 3-Methylindole (3MI) is a naturally occurring pulmonary toxin that requires metabolic activation. In particular, 3MI-induced pneumotoxicity arises from cytochrome P-450-catalyzed dehydrogenation of 3MI to an electrophilic methylene imine (3-methyleneindolenine), which covalently binds to cellular macromolecules. Members of the CYP2F gene subfamily are selectively expressed in lung tissues and have been implicated as important catalysts in the formation of reactive intermediates from several pneumotoxic chemicals. (PMID: 10383923) [HMDB] 3-Methylene-indolenine is an electrophilic molecule produced by the action of cytochrome P450 2F1 on 3-methylindole (3MI). 3-Methylindole (3MI) is a naturally occurring pulmonary toxin that requires metabolic activation. In particular, 3MI-induced pneumotoxicity arises from cytochrome P-450-catalyzed dehydrogenation of 3MI to an electrophilic methylene imine (3-methyleneindolenine), which covalently binds to cellular macromolecules. Members of the CYP2F gene subfamily are selectively expressed in lung tissues and have been implicated as important catalysts in the formation of reactive intermediates from several pneumotoxic chemicals. (PMID: 10383923).

   

3-Phenyl-2-propenenitrile

(2Z)-3-phenylprop-2-enenitrile

C9H7N (129.0578462)


3-phenyl-2-propenenitrile is a member of the class of compounds known as styrenes. Styrenes are organic compounds containing an ethenylbenzene moiety. 3-phenyl-2-propenenitrile is a cassia, cinnamon, and cumin tasting compound found in fig, which makes 3-phenyl-2-propenenitrile a potential biomarker for the consumption of this food product.

   

Nitrile-(E)-3-Phenyl-2-propenoic acid

Nitrile-(E)-3-Phenyl-2-propenoic acid

C9H7N (129.0578462)


   

Quinoline; AIF; CE0; CorrDec

Quinoline; AIF; CE0; CorrDec

C9H7N (129.0578462)


   

Quinoline; AIF; CE10; CorrDec

Quinoline; AIF; CE10; CorrDec

C9H7N (129.0578462)


   

Quinoline; AIF; CE30; CorrDec

Quinoline; AIF; CE30; CorrDec

C9H7N (129.0578462)


   

Quinoline; AIF; CE0; MS2Dec

Quinoline; AIF; CE0; MS2Dec

C9H7N (129.0578462)


   

Quinoline; AIF; CE30; MS2Dec

Quinoline; AIF; CE30; MS2Dec

C9H7N (129.0578462)


   

Quinoline; LC-tDDA; CE10

Quinoline; LC-tDDA; CE10

C9H7N (129.0578462)


   

Quinoline; LC-tDDA; CE20

Quinoline; LC-tDDA; CE20

C9H7N (129.0578462)


   

Quinoline; LC-tDDA; CE30

Quinoline; LC-tDDA; CE30

C9H7N (129.0578462)


   

Quinoline; LC-tDDA; CE40

Quinoline; LC-tDDA; CE40

C9H7N (129.0578462)


   

3-Methyleneindolenine

3-Methylene-indolenine

C9H7N (129.0578462)


An indole that consists of 3H-indole bearing a methylene substituent at position 3.

   

4-CYANOSTYRENE

4-CYANOSTYRENE

C9H7N (129.0578462)


   

Cinnamonitrile

Cinnamonitrile

C9H7N (129.0578462)


   

Bicyclo[4.2.0]octa-1,3,5-triene-7-carbonitrile

Bicyclo[4.2.0]octa-1,3,5-triene-7-carbonitrile

C9H7N (129.0578462)


   

(Z)-3-Phenylacrylonitrile

(Z)-3-Phenylacrylonitrile

C9H7N (129.0578462)


   

Leucol

InChI=1\C9H7N\c1-2-6-9-8(4-1)5-3-7-10-9\h1-7

C9H7N (129.0578462)


   

3-[(E)-but-1-en-3-ynyl]pyridine

3-[(E)-but-1-en-3-ynyl]pyridine

C9H7N (129.0578462)


   
   

ISOQUINOLINE

ISOQUINOLINE

C9H7N (129.0578462)