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CAS 55332-37-1

:

(2S)-2-(4-fluorophenyl)-3-methylbutanoic acid

Description:
(2S)-2-(4-fluorophenyl)-3-methylbutanoic acid, with the CAS number 55332-37-1, is a chiral compound characterized by its specific stereochemistry, indicated by the (2S) designation. This compound features a butanoic acid backbone, which includes a methyl group and a 4-fluorophenyl substituent. The presence of the fluorine atom on the phenyl ring can influence the compound's biological activity and lipophilicity, potentially enhancing its pharmacological properties. As a carboxylic acid, it exhibits typical acidic behavior, including the ability to donate protons in solution. The compound's chirality may lead to different biological activities for its enantiomers, making it of interest in medicinal chemistry. Its structural features suggest potential applications in pharmaceuticals, particularly in the development of drugs targeting specific biological pathways. Additionally, the compound's solubility, stability, and reactivity can be influenced by its functional groups and overall molecular structure, which are important considerations in both synthetic and analytical chemistry contexts.
Formula:C11H13FO2
InChI:InChI=1/C11H13FO2/c1-7(2)10(11(13)14)8-3-5-9(12)6-4-8/h3-7,10H,1-2H3,(H,13,14)/t10-/m0/s1
SMILES:CC(C)[C@@H](c1ccc(cc1)F)C(=O)O
Synonyms:
  • benzeneacetic acid, 4-fluoro-α-(1-methylethyl)-, (alphaS)-
  • (S)-2-(4-fluorophenyl)-3-methylbutanoic acid
  • (2S)-2-(4-fluorophenyl)-3-methylbutanoic acid
  • Benzeneacetic acid, 4-fluoro-α-(1-methylethyl)-, (αS)-
  • (S)-.alpha.-Isopropyl-p-fluorophenylacetic acid
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