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CAS 939-89-9

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(1R,2S)-2-phenylcyclopropanecarboxylic acid

Description:
(1R,2S)-2-phenylcyclopropanecarboxylic acid is a chiral compound characterized by its cyclopropane ring structure, which is substituted with a phenyl group and a carboxylic acid functional group. The specific stereochemistry indicated by the (1R,2S) notation refers to the spatial arrangement of atoms around the chiral centers, influencing its biological activity and reactivity. This compound typically appears as a white to off-white solid and is soluble in organic solvents, with limited solubility in water due to the hydrophobic phenyl group. Its carboxylic acid functionality allows it to participate in various chemical reactions, such as esterification and acid-base reactions. The compound may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Additionally, its unique structure can lead to specific interactions with biological targets, which is valuable in drug design and development. As with many organic compounds, proper handling and storage are essential to maintain its stability and prevent degradation.
Formula:C10H10O2
InChI:InChI=1/C10H10O2/c11-10(12)9-6-8(9)7-4-2-1-3-5-7/h1-5,8-9H,6H2,(H,11,12)/t8-,9-/m1/s1
SMILES:c1ccc(cc1)[C@H]1C[C@H]1C(=O)O
Synonyms:
  • cyclopropanecarboxylic acid, 2-phenyl-, (1R,2S)-
  • (1R,2S)-2-Phenylcyclopropanecarboxylic acid
  • (1R,2S)‐rel-2‐phenylcyclopropane‐1‐carboxylic acid
  • cis-2-phenylcyclopropane-1-carboxylic acid
  • rel-(1R,2S)-2-Phenylcyclopropanecarboxylic Acid
  • rel-((1S,2R)-2-Phenylcyclopropane-1-carboxylic acid)
  • (1S*,2R*)-2-phenylcyclopropane-1-carboxylic acid
  • -rel-2-Phenylcyclopropanecarboxylic acid
  • CYCLOPROPANECARBOXYLIC ACID,2-PHENYL-,(1R,2S)-REL-
  • (1R,2S)-rel-2-Phenylcyclopropanecarboxylic acid
  • cis-2-Phenylcyclopropanecarboxylicacid
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