Description

Cyclopropyl(phenyl)methanamine (CAS No. 23459-38-3) is a high-purity organic compound with the molecular formula C₁₀H₁₃N. This chiral amine features a cyclopropyl group and a phenyl ring attached to a central methanamine moiety, making it a valuable intermediate in pharmaceutical synthesis and medicinal chemistry research. Our product is rigorously tested for purity and consistency, ensuring optimal performance in demanding applications. Available in various enantiomeric forms, including (S)- and (R)-configurations, as well as racemic mixtures and hydrochloride salts, this compound is supplied with comprehensive analytical documentation (HPLC, GC-MS, NMR) to meet the stringent requirements of research and industrial applications.

Properties

• CAS Number: 23459-38-3
• Complexity: 123
• IUPAC Name: cyclopropyl(phenyl)methanamine
• InChI: InChI=1S/C10H13N/c11-10(9-6-7-9)8-4-2-1-3-5-8/h1-5,9-10H,6-7,11H2
• InChI Key: UCRSQPUGEDLYSH-UHFFFAOYSA-N
• Exact Mass: 147.104799419
• Molecular Formula: C10H13N
• Molecular Weight: 147.22
• SMILES: C1CC1C(C2=CC=CC=C2)N
• Topological: 26
• Monoisotopic Mass: 147.104799419
• Synonyms: cyclopropyl(phenyl)methanamine, 23459-38-3, DTXSID60391007, DTXCID40341868, 809-062-0, 1-cyclopropyl-1-phenylmethanamine, (S)-cyclopropyl(phenyl)methanamine, MFCD05191945, Benzenemethanamine, alpha-cyclopropyl-, (S)-C-Cyclopropyl-C-phenyl-methylamine, (R)-C-Cyclopropyl-C-phenyl-methylamine, Cyclopropyl(phenyl)methanamine HCl, C-CYCLOPROPYL-C-PHENYL-METHYLAMINE, (s)-1-cyclopropyl-1-phenylmethanamine, (1R)-1-CYCLOPROPYL-1-PHENYLMETHANAMINE, alpha-cyclopropylbenzylamine, 155047-88-4, rac-alpha-cyclopropylbenzylamine, a-Cyclopropyl-benzenemethanamine, SCHEMBL1423740, SCHEMBL4926694, SCHEMBL6635629, SCHEMBL6641093, SCHEMBL16935660, UCRSQPUGEDLYSH-UHFFFAOYSA-N, Benzenemethanamine, |A-cyclopropyl-, AKOS000199754, AKOS016344064, SB36582, SB37181, BS-13453, SY042927, CS-0449873, EN300-30475, F14028

Cyclopropyl(phenyl)methanamine serves as a key building block in the synthesis of bioactive molecules, particularly in the development of CNS-active compounds and enzyme inhibitors. Its rigid cyclopropyl group enhances conformational restriction in drug candidates, improving target selectivity. Researchers utilize this amine in asymmetric synthesis, ligand design, and as a precursor for novel heterocyclic systems. The hydrochloride salt form is particularly useful for improving solubility in aqueous reaction conditions.

Safety and Hazards

GHS Hazard Statements

• H301 (98.5%): Toxic if swallowed [Danger Acute toxicity, oral]

Precautionary Statements

• P264, P270, P301+P316, P321, P330, P405, and P501

Hazard Classes and Categories

• Acute Tox. 3 (98.5%)

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