Exact Mass: 142.0005532

Exact Mass Matches: 142.0005532

Found 59 metabolites which its exact mass value is equals to given mass value 142.0005532, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

2-Thienylacetic acid

2-Thiopheneacetic acid

C6H6O2S (142.0088496)


   

2,2-Dichlorethyl ether

1,5-Dichloro-3-oxapentane

C4H8Cl2O (141.9952178)


   

Alloxan

2,4,5,6-Tetraoxohexahydropyrimidine

C4H2N2O4 (142.0014572)


Alloxan or mesoxalylurea is an organic compound based on a pyrimidine heterocyclic skeleton. This compound has a high affinity for water and therefore exists as the monohydrate. The compound was discovered by Justus von Liebig and Friedrich Wohler following the discovery of urea in 1828 and is one of the oldest named organic compounds that exist. The name is derived from allantoin, a product of uric acid excreted by the fetus into the allantois and oxaluric acid derived from oxalic acid and urea, found in urine. The original recipe for Alloxan was by oxidation of uric acid by nitric acid. Alloxan is a strong oxidizing agent and it forms a hemiacetal with its reduced reaction product dialuric acid (in which a carbonyl group is reduced to a hydroxyl group) which is called alloxantin. -- Wikipedia; Alloxane is a raw material for the production of the purple dye Murexide. Carl Wilhelm Scheele discovered the dye in 1776. Murexide is the product of the complex in-situ multistep reaction of alloxantin and gaseous ammonia. Murexide results from the condensation of the unisolated intermdiate uramil with alloxan, liberated during the course of the reaction. Scheele sourced uric acid from human calculi (such as kidney stones) and called the compound lithic acid. William Prout investigated the compound in 1818 and he used boa constrictor excrement with up to 90\\% ammonium acid urate. Liebig and Wohler in the nineteenth century coined the name murexide for the dye after the Trunculus Murex which is the source of the Tyrian purple of antiquity. Primo Levi in his world famous novel The Periodic Table in chapter Nitrogen considers pythons as a source for alloxane on behalf of a lipstick producer but he is turned down by the director of the Turin zoo because the zoo already has lucrative contracts with cosmetics companies (his attempts with chicken dung end in misery). -- Wikipedia [HMDB] Alloxan or mesoxalylurea is an organic compound based on a pyrimidine heterocyclic skeleton. This compound has a high affinity for water and therefore exists as the monohydrate. The compound was discovered by Justus von Liebig and Friedrich Wohler following the discovery of urea in 1828 and is one of the oldest named organic compounds that exist. The name is derived from allantoin, a product of uric acid excreted by the fetus into the allantois and oxaluric acid derived from oxalic acid and urea, found in urine. The original recipe for Alloxan was by oxidation of uric acid by nitric acid. Alloxan is a strong oxidizing agent and it forms a hemiacetal with its reduced reaction product dialuric acid (in which a carbonyl group is reduced to a hydroxyl group) which is called alloxantin. -- Wikipedia; Alloxane is a raw material for the production of the purple dye Murexide. Carl Wilhelm Scheele discovered the dye in 1776. Murexide is the product of the complex in-situ multistep reaction of alloxantin and gaseous ammonia. Murexide results from the condensation of the unisolated intermdiate uramil with alloxan, liberated during the course of the reaction. Scheele sourced uric acid from human calculi (such as kidney stones) and called the compound lithic acid. William Prout investigated the compound in 1818 and he used boa constrictor excrement with up to 90\\% ammonium acid urate. Liebig and Wohler in the nineteenth century coined the name murexide for the dye after the Trunculus Murex which is the source of the Tyrian purple of antiquity. Primo Levi in his world famous novel The Periodic Table in chapter Nitrogen considers pythons as a source for alloxane on behalf of a lipstick producer but he is turned down by the director of the Turin zoo because the zoo already has lucrative contracts with cosmetics companies (his attempts with chicken dung end in misery). -- Wikipedia.

   

Methyl thiophene-2-carboxylate

2-Thiophenecarboxylic acid, methyl ester

C6H6O2S (142.0088496)


Methyl thiophene-2-carboxylate is a maillard produc

   

S-(2-Furanylmethyl) methanethioate

Methanethioic acid, 3-(2-furanylmethyl) ester

C6H6O2S (142.0088496)


S-(2-Furanylmethyl) methanethioate is a flavouring ingredient. Flavouring ingredient

   

Methyl 2-thiofuroate

2-Furancarbothioic acid, S-methyl ester

C6H6O2S (142.0088496)


Methyl 2-thiofuroate is a flavouring ingredient with a fried, cooked onion odour. Flavouring ingredient with a fried, cooked onion odour

   

1,2-Benzenedithiol

benzene-1,2-dithiol

C6H6S2 (141.9910916)


   

Benzenesulfinic acid

(R)-benzenesulfinic acid

C6H6O2S (142.0088496)


   

Isopropyldichloromethyl ether

Isopropyldichloromethyl ether

C4H8Cl2O (141.9952178)


   

Phenylsulfinic acid

BENZENESULFINIC ACID

C6H6O2S (142.0088496)


   

3-Methyl-2-thiophenecarboxylic acid

3-Methyl-2-thiophenecarboxylic acid

C6H6O2S (142.0088496)


   

Alloxan

Alloxan

C4H2N2O4 (142.0014572)


A member of the class of pyrimidones, the structure of which is that of perhydropyrimidine substituted at C-2, -4, -5 and -6 by oxo groups.

   

Methyl thenoate

2-Thiophenecarboxylic acid, methyl ester

C6H6O2S (142.0088496)


   

Furfuryl thioformate

Methanethioic acid, 3-(2-furanylmethyl) ester

C6H6O2S (142.0088496)


   

Methyl thiofuroate

2-Furancarbothioic acid, S-methyl ester

C6H6O2S (142.0088496)


   

3-chloropropanimidamide,hydrochloride

3-chloropropanimidamide,hydrochloride

C3H8Cl2N2 (142.0064508)


   

Methyl 2-thiophenecarboxylate

Methyl 2-thiophenecarboxylate

C6H6O2S (142.0088496)


   

5-Chloropyrazine-2-carbaldehyde

5-Chloropyrazine-2-carbaldehyde

C5H3ClN2O (141.9933898)


   

2-hydroxy-1-thiophen-2-ylethanone

2-hydroxy-1-thiophen-2-ylethanone

C6H6O2S (142.0088496)


   

6-chloropyridazine-3-carbaldehyde

6-chloropyridazine-3-carbaldehyde

C5H3ClN2O (141.9933898)


   

2-Chloro-5-pyrimidinecarbaldehyde

2-Chloro-5-pyrimidinecarbaldehyde

C5H3ClN2O (141.9933898)


   

5-Methyl-3-thiophenecarboxylic acid

5-Methyl-3-thiophenecarboxylic acid

C6H6O2S (142.0088496)


   

2,3,5,6-Piperazinetetrone

2,3,5,6-Piperazinetetrone

C4H2N2O4 (142.0014572)


   

2-Butanol,1,4-dichloro-

2-Butanol,1,4-dichloro-

C4H8Cl2O (141.9952178)


   

6-Chloro-4-pyrimidinecarbaldehyde

6-Chloro-4-pyrimidinecarbaldehyde

C5H3ClN2O (141.9933898)


   

3-Chloro-2-pyrazinecarbaldehyde

3-Chloro-2-pyrazinecarbaldehyde

C5H3ClN2O (141.9933898)


   

1-(3-hydroxythiophen-2-yl)ethanone

1-(3-hydroxythiophen-2-yl)ethanone

C6H6O2S (142.0088496)


   

3-Thienylacetic acid

3-Thienylacetic acid

C6H6O2S (142.0088496)


   

3,4-Ethylenedioxythiophene

3,4-Ethylenedioxythiophene

C6H6O2S (142.0088496)


   

5-Methly-2-thiophenecarboxylic acid

5-Methly-2-thiophenecarboxylic acid

C6H6O2S (142.0088496)


   

3-Methoxythiophene-2-carbaldehyde

3-Methoxythiophene-2-carbaldehyde

C6H6O2S (142.0088496)


   

5-Pyrimidinecarbonyl chloride

5-Pyrimidinecarbonyl chloride

C5H3ClN2O (141.9933898)


   

2-pyrazinecarbonyl chloride

2-pyrazinecarbonyl chloride

C5H3ClN2O (141.9933898)


   

2-Pyrimidinecarbonyl chloride (9CI)

2-Pyrimidinecarbonyl chloride (9CI)

C5H3ClN2O (141.9933898)


   

Chloropyrimidine-5-carbaldehyde

Chloropyrimidine-5-carbaldehyde

C5H3ClN2O (141.9933898)


   

4-Chloro-2-pyrimidinecarbaldehyde

4-Chloro-2-pyrimidinecarbaldehyde

C5H3ClN2O (141.9933898)


   

1,4-BENZENEDITHIOL

1,4-BENZENEDITHIOL

C6H6S2 (141.9910916)


   

chlorophenylsilane

chlorophenylsilane

C6H7ClSi (142.0005532)


   

1,2-Dichloro-1-ethoxyethane

1,2-Dichloro-1-ethoxyethane

C4H8Cl2O (141.9952178)


   

2,5-Dihydroxythiophenol

2,5-Dihydroxythiophenol

C6H6O2S (142.0088496)


   

4-Methylthiophene-3-carboxylic acid

4-Methylthiophene-3-carboxylic acid

C6H6O2S (142.0088496)


   

1,3-benzenedithiol

1,3-benzenedithiol

C6H6S2 (141.9910916)


   

Potassium 3-hydroxybutyrate

Potassium 3-hydroxybutyrate

C4H7KO3 (142.0032252)


   

potassium(R) 3-hydroxybutyrate

potassium(R) 3-hydroxybutyrate

C4H7KO3 (142.0032252)


   

PYRIMIDINE-4-CARBONYLCHLORIDE

PYRIMIDINE-4-CARBONYLCHLORIDE

C5H3ClN2O (141.9933898)


   

4-methoxy-thiophene-2-carboxaldehyde

4-methoxy-thiophene-2-carboxaldehyde

C6H6O2S (142.0088496)


   

Methyl thiophene-3-carboxylate

Methyl thiophene-3-carboxylate

C6H6O2S (142.0088496)


   

2-chloropyrimidine-4-carbaldehyde

2-chloropyrimidine-4-carbaldehyde

C5H3ClN2O (141.9933898)


   

2-Methylthiophene-3-carboxylic acid

2-Methylthiophene-3-carboxylic acid

C6H6O2S (142.0088496)


   

6-Chloro-2-pyrazinecarbaldehyde

6-Chloro-2-pyrazinecarbaldehyde

C5H3ClN2O (141.9933898)


   

5-methoxythiophene-2-carbaldehyde

5-methoxythiophene-2-carbaldehyde

C6H6O2S (142.0088496)


   

5-chloropyrimidine-2-carbaldehyde

5-chloropyrimidine-2-carbaldehyde

C5H3ClN2O (141.9933898)


   

2-Hydroxyethyl phosphate

2-Hydroxyethyl phosphate

C2H7O5P (142.0031102)


   

1,2-Dihydroxyethylphosphonic acid

1,2-Dihydroxyethylphosphonic acid

C2H7O5P (142.0031102)


   
   

Methyl thiophene-2-carboxylate

Methyl thiophene-2-carboxylate

C6H6O2S (142.0088496)


   

Methyl 2-thiofuroate

2-(Carbomethoxy)thiophene

C6H6O2S (142.0088496)


   
   

Thienylacetic acid

Thienylacetic acid

C6H6O2S (142.0088496)