CAS 74431-52-0
:(2R)-3-(Acetylthio)-2-methylpropanoic acid
Description:
(2R)-3-(Acetylthio)-2-methylpropanoic acid, with the CAS number 74431-52-0, is an organic compound characterized by its unique functional groups and stereochemistry. This compound features a propanoic acid backbone, which includes a methyl group and an acetylthio group attached to the second and third carbon atoms, respectively. The presence of the acetylthio group introduces a thiol functional group, which can influence the compound's reactivity and solubility. As a chiral molecule, it exists in two enantiomeric forms, with the (2R) designation indicating the specific spatial arrangement of its atoms. This stereochemistry can affect its biological activity and interactions with other molecules. The compound is likely to be soluble in polar solvents due to the carboxylic acid group, while the presence of the thioether may impart additional properties relevant to its reactivity. Overall, (2R)-3-(Acetylthio)-2-methylpropanoic acid is of interest in various fields, including medicinal chemistry and biochemistry, due to its potential applications and unique structural features.
Formula:C6H10O3S
InChI:InChI=1S/C6H10O3S/c1-4(6(8)9)3-10-5(2)7/h4H,3H2,1-2H3,(H,8,9)/t4-/m0/s1
InChI key:InChIKey=VFVHNRJEYQGRGE-BYPYZUCNSA-N
SMILES:[C@H](CSC(C)=O)(C(O)=O)C
Synonyms:- (2R)-3-(Acetylthio)-2-methylpropanoic acid
- (2R)-3-(acetylsulfanyl)-2-methylpropanoic acid
- Propanoic acid, 3-(acetylthio)-2-methyl-, (2R)-
- Propanoic acid, 3-(acetylthio)-2-methyl-, (R)-
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