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CAS 63640-09-5

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(2R)-2-(4-chlorophenyl)-3-methylbutanoic acid

Description:
(2R)-2-(4-chlorophenyl)-3-methylbutanoic acid, also known as a chiral compound, is characterized by its specific stereochemistry, indicated by the (2R) configuration at the second carbon atom. This compound features a butanoic acid backbone with a methyl group at the third carbon and a para-chlorophenyl group at the second carbon, contributing to its unique properties. The presence of the chlorophenyl group enhances its lipophilicity, potentially affecting its biological activity and interactions with various receptors or enzymes. As a carboxylic acid, it exhibits acidic properties, capable of donating a proton in solution, which can influence its solubility and reactivity. The compound's chirality may also play a significant role in its pharmacological effects, as different enantiomers can exhibit different biological activities. Overall, (2R)-2-(4-chlorophenyl)-3-methylbutanoic acid is of interest in medicinal chemistry and pharmacology, particularly in the development of drugs with specific therapeutic targets.
Formula:C11H13ClO2
InChI:InChI=1/C11H13ClO2/c1-7(2)10(11(13)14)8-3-5-9(12)6-4-8/h3-7,10H,1-2H3,(H,13,14)/t10-/m1/s1
SMILES:CC(C)[C@H](c1ccc(cc1)Cl)C(=O)O
Synonyms:
  • benzeneacetic acid, 4-chloro-alpha-(1-methylethyl)-, (alphaR)-
  • (R)-2-(4-Chloro-Phenyl)-3-Methyl-Butyric Acid
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