(1R,2S)-2-(3,4-Difluorophenyl)cyclopropanamine (2R)-Hydroxy(phenyl)ethanoate

• CAT Number: R057194
• CAS Number: 376608-71-8
• Molecular Formula: C17H17F2NO3
• Molecular Weight: 321.32
• Purity: ≥95%
• Synonyms: (αR)-α-Hydroxybenzeneacetic Acid compd. with (1R,2S)-2-(3,4-Difluorophenyl)cyclopropanamine
• Storage: -20°C
• IUPAC Name: (1R,2S)-2-(3,4-difluorophenyl)cyclopropan-1-amine;(2R)-2-hydroxy-2-phenylacetic acid
• InChI: InChI=1S/C9H9F2N.C8H8O3/c10-7-2-1-5(3-8(7)11)6-4-9(6)12;9-7(8(10)11)6-4-2-1-3-5-6/h1-3,6,9H,4,12H2;1-5,7,9H,(H,10,11)/t6-,9+;7-/m01/s1
• InChIKey: GUESUQPLVFMJIT-KLTOLQSASA-N
• SMILES: C1[C@H]([C@@H]1N)C2=CC(=C(C=C2)F)F.C1=CC=C(C=C1)[C@H](C(=O)O)O

(1R,2S)-2-(3,4-Difluorophenyl)cyclopropanamine (2R)-hydroxy(phenyl)ethanoate（Cat No.:R057194）is a chiral pharmaceutical intermediate or active compound featuring both cyclopropane and phenylethanoate moieties. The cyclopropanamine core with a 3,4-difluorophenyl substituent offers structural rigidity and potential bioactivity, often enhancing receptor selectivity and metabolic stability. The (2R)-hydroxy(phenyl)ethanoate portion resembles structures found in bioactive molecules, contributing to interactions with enzymes or receptors. This compound may be used in drug development, particularly in CNS or cardiovascular research, due to its stereochemistry and pharmacophoric groups. Its dual chiral centers provide specificity in biological targeting and pharmacological response.