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CAS 26782-75-2

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

Description:
(2S)-2-Bromo-3-methylbutanoic acid is an organic compound characterized by its chiral center, which imparts specific stereochemical properties. It features a bromine atom attached to the second carbon of a butanoic acid backbone, along with a methyl group on the third carbon. This configuration contributes to its potential applications in asymmetric synthesis and as an intermediate in pharmaceutical chemistry. The presence of the carboxylic acid functional group (-COOH) indicates that it can participate in acid-base reactions and can form salts or esters. The bromine substituent enhances its reactivity, making it useful in nucleophilic substitution reactions. Additionally, the compound's chirality may influence its biological activity, making it of interest in the development of chiral drugs. Its physical properties, such as solubility and boiling point, are influenced by the molecular structure and the presence of functional groups. Overall, (2S)-2-Bromo-3-methylbutanoic acid is a valuable compound in organic synthesis and medicinal chemistry due to its unique structural features.
Formula:C5H9BrO2
InChI:InChI=1S/C5H9BrO2/c1-3(2)4(6)5(7)8/h3-4H,1-2H3,(H,7,8)/t4-/m0/s1
InChI key:InChIKey=UEBARDWJXBGYEJ-BYPYZUCNSA-N
SMILES:[C@H](C(C)C)(C(O)=O)Br
Synonyms:
  • (-)-2-Bromo-3-methylbutyric acid
  • (2R)-2-bromo-3-methylbutanoic acid
  • (2S)-2-bromo-3-methylbutanoic acid
  • (S)-2-Bromo-3-methylbutanoic acid
  • (S)-2-Bromoisovaleric acid
  • Butanoic acid, 2-bromo-3-methyl-, (2S)-
  • Butanoic acid, 2-bromo-3-methyl-, (S)-
  • Butyric acid, 2-bromo-3-methyl-, (S)-
  • S-2-Bromo-3-methylbutyric acid
  • (S)-2-Bromo-3-methylbutyric acid
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