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Methyl thioglycolate

Catalog Number
ACM2365482
Product Name
Methyl thioglycolate
Structure
Methyl thioglycolate
CAS
2365-48-2
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Synonyms
RP18865; methyl-2-mercaptoacetate; Methyl sulfanylacetate #; mercapto-acetic acid methylester; NSC-75117; 2365-48-2; MCULE-3020830180; Acetic acid, 2-mercapto-, methyl ester; TRA0039347; Thioglykolsaeure-methylester;
IUPAC Name
methyl 2-sulfanylacetate;
Molecular Weight
106.139g/mol
Molecular Formula
C3H6O2S;
InChI
InChI=1S/C3H6O2S/c1-5-3(4)2-6/h6H,2H2,1H3;
InChI Key
MKIJJIMOAABWGF-UHFFFAOYSA-N;
Storage
Store below +30°C.
Complexity
52.8
Covalently-Bonded Unit Count
1
Decomposition
When heated to decomposition it emits toxic fumes of sulfoxides.;
EC Number
219-121-7
Exact Mass
106.009g/mol
H-Bond Acceptor
3
H-Bond Donor
1
Heavy Atom Count
6
Monoisotopic Mass
106.009g/mol
NSC Number
75117
Rotatable Bond Count
2
Topological Polar Surface Area
27.3A^2
Undefined Atom Stereocenter Count
1
UNII
O1608LA9EL
Vapor Pressure
3.00 mmHg;
Application
Methyl Thioglycolate is an derivative of Thioglycolic Acid (T350760), an organic compound containing both a thiol and a carboxylic acid functional groups. Thioglycolic Acid and its derivatives are often used in organic synthesis as a nucleophile in thioglycolysis reactions and is also used as a S transfer agent for sulfonyl chloride synthesis. Methyl Thioglycolate have been studied for the its influence on neocarzinostatin activation and expression of DNA damage.
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