
CAS 111058-32-3: Methyl (2R)-2-oxiranecarboxylate
Formula:C4H6O3
InChI:InChI=1S/C4H6O3/c1-6-4(5)3-2-7-3/h3H,2H2,1H3/t3-/m1/s1
InChI key:InChIKey=YKNYRRVISWJDSR-GSVOUGTGSA-N
SMILES:C(OC)(=O)[C@H]1CO1
Synonyms:- (2R)-Oxirane-2-Carboxylic Acid Methyl Ester
- (R)-Glycidic acid methyl ester
- (R)-Methyl glycidate
- 2-Oxiranecarboxylic acid methyl ester (2R)-
- Methyl (2R)-2-oxiranecarboxylate
- Methyl (2R)-Glycidate 97% (94% Ee/Glc)
- Methyl (2R)-Oxirane-2-Carboxylate
- Methyl (2R)-glycidate
- Methyl (R)-Oxiranecarboxylate
- Oxiranecarboxylic acid, methyl ester, (2R)-
- Oxiranecarboxylic acid, methyl ester, (R)-
- See more synonyms
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Found 5 products.
(R)-Glycidic Acid Methyl Ester
CAS:Controlled ProductApplications Used in the preparation of antibacterial oxazolidinones. References Kim, J. et al.: 19, 550 (2009); Michael R. et al.: J. Med. Chem., 50, 5886 (2007)Formula:C4H6O3Color and Shape:NeatMolecular weight:102.09(R)-Methyl oxirane-2-carboxylate
CAS:Purity:95.0%Color and Shape:Liquid, No data available.Molecular weight:102.08899688720703(R)-Methyglycidate
CAS:(R)-Methyglycidate is a synthetic compound that has been shown to be effective in inhibiting the activity of cerebral, mediated, and acetonitrile-mediated lipases. The demethylation of (R)-methyglycidate is catalyzed by superacidic conditions present at pH 0.1. The alkylation with trifluoromethanesulfonic acid leads to inhibition of gelatinase and lipase activities. This compound has also been shown to have inhibitory effects on enzymes involved in cerebral inflammation, including glutamate decarboxylase, phospholipases A2, and cyclooxygenases. These inhibitory effects may be due to the inhibition of arachidonic acid release from phospholipids.Formula:C4H6O3Purity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:102.09 g/molRef: 3D-FM16255
Discontinued product