(S)-3-Cyclohexene-1-carboxylic Acid

• CAT Number: R023479
• CAS Number: 5708-19-0
• Molecular Formula: C7H10O2
• Molecular Weight: 126.16
• Purity: ≥95%
• Synonyms: (S)-(-)-3-Cyclohexene-1-carboxylic Acid; (S)-3-Cyclohexene-1-carboxylic Acid
• Storage: Desiccate at -20°C
• IUPAC Name: (1S)-cyclohex-3-ene-1-carboxylic acid
• InChI: InChI=1S/C7H10O2/c8-7(9)6-4-2-1-3-5-6/h1-2,6H,3-5H2,(H,8,9)/t6-/m1/s1
• InChIKey: VUSWCWPCANWBFG-ZCFIWIBFSA-N
• SMILES: C1CC(CC=C1)C(=O)O

(S)-3-Cyclohexene-1-carboxylic acid(CAT: R023479) is a chiral cyclic carboxylic acid featuring a cyclohexene ring with a carboxyl group at the 1-position in the (S)-enantiomeric form. The unsaturated ring structure provides both rigidity and synthetic versatility, making it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and fine chemicals. Its chirality enables enantioselective synthesis of biologically active compounds, including intermediates for natural products and medicinal agents. The compound can undergo diverse chemical transformations such as esterification, amidation, and hydrogenation, allowing structural diversification for structure–activity relationship (SAR) studies in drug discovery and advanced organic synthesis.