CAS 733740-94-8

(1R,2R)-2-(4-ethylbenzoyl)cyclopentane-1-carboxylic acid

Description:

(1R,2R)-2-(4-ethylbenzoyl)cyclopentane-1-carboxylic acid is a chiral compound characterized by its cyclopentane ring structure, which is substituted with a carboxylic acid group and a 4-ethylbenzoyl moiety. The presence of the carboxylic acid functional group imparts acidic properties, allowing it to participate in acid-base reactions. The compound's chirality, indicated by the (1R,2R) configuration, suggests that it exists as a specific stereoisomer, which can influence its biological activity and interactions with other molecules. The 4-ethylbenzoyl group contributes to the compound's hydrophobic characteristics, potentially affecting its solubility and reactivity in various solvents. This compound may be of interest in pharmaceutical research and organic synthesis due to its unique structural features and potential applications in drug development. Its CAS number, 733740-94-8, allows for easy identification and reference in chemical databases and literature. Overall, the compound's distinct structural and functional characteristics make it a subject of interest in the field of organic chemistry.

Formula: C₁₅H₁₈O₃

InChI: InChI=1/C15H18O3/c1-2-10-6-8-11(9-7-10)14(16)12-4-3-5-13(12)15(17)18/h6-9,12-13H,2-5H2,1H3,(H,17,18)/t12-,13-/m1/s1

SMILES: CCc1ccc(cc1)C(=O)[C@@H]1CCC[C@H]1C(=O)O

Synonyms:

• Cyclopentanecarboxylic acid, 2-(4-ethylbenzoyl)-, (1R,2R)-rel-
• (1R,2R)-2-(4-ethylbenzoyl)cyclopentane-1-carboxylic acid
• TRANS-2-(4-ETHYLBENZOYL)CYCLOPENTANE-1-CARBOXYLIC ACID