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CAS 26782-74-1

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(2S)-2-Chloro-3-methylbutanoic acid

Description:
(2S)-2-Chloro-3-methylbutanoic acid is an organic compound characterized by its chiral center, which contributes to its specific stereochemistry. It features a chloro substituent at the second carbon and a methyl group at the third carbon of a butanoic acid backbone. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in polar solvents like water and alcohols, owing to the presence of the carboxylic acid functional group, which can engage in hydrogen bonding. The chloro group introduces reactivity, making it a potential intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its chiral nature allows for the exploration of its enantiomers in various applications, as different stereoisomers can exhibit distinct biological activities. Safety considerations include handling it with care due to its potential toxicity and reactivity, particularly in the presence of strong bases or nucleophiles. Proper storage and disposal methods should be followed to mitigate environmental and health risks.
Formula:C5H9ClO2
InChI:InChI=1/C5H9ClO2/c1-3(2)4(6)5(7)8/h3-4H,1-2H3,(H,7,8)/t4-/m0/s1
InChI key:InChIKey=DDTJFSPKEIAZAM-BYPYZUCNSA-N
SMILES:[C@H](C(C)C)(C(O)=O)Cl
Synonyms:
  • (2S)-2-chloro-3-methylbutanoic acid
  • (S)-(+)-2-Chloro-3-methylbutanoic acid
  • Butanoic acid, 2-chloro-3-methyl-, (2S)-
  • Butanoic acid, 2-chloro-3-methyl-, (S)-
  • Butyric acid, 2-chloro-3-methyl-, (S)-
  • S-2-chloro-3-methylbutyric acid
  • (S)-(-)-2-Chloro-3-methylbutyric acid
  • (S)-2-CHLOROISOVALERIC ACID
  • (S)-2-CHLORO-3-METHYLBUTYRIC ACID GC 97+%
  • (S)-ALPHA-CHLOROISOVALERIC ACID
  • (s)-α-chloroisovaleric acid
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