(R)-(+)-N-Benzyl-1-phenylethylamine

CAS: 38235-77-7

Ref. 3D-FB11207

Product Information

• Name: (R)-(+)-N-Benzyl-1-phenylethylamine
• Synonyms: (+)-Benzylphenethylamine, (+)-N-Benzyl-1-phenylethylamine, (+)-N-Benzyl-α-phenylethylamine, (1R)-N-(cyclohexylmethyl)-1-phenylethanaminium, (R)-(+)-N-Benzyl-α-methylbenzylamine, (R)-Benzyl(α-methylbenzyl)amine, (R)-N-(α-Methylbenzyl)-N-benzylamine, (R)-N-Benzyl-1-phenyl-1-ethylamine, (R)-N-Benzyl-1-phenylethan-1-amine, (R)-N-Benzyl-1-phenylethanamine, (R)-N-Benzyl-N-(-methylbenzyl)amine, (R)-N-Benzyl-N-α-methylbenzylamine, (αR)-α-Methyl-N-(phenylmethyl)benzenemethanamine, Benzenemethanamine, α-methyl-N-(phenylmethyl)-, (R)-, Benzenemethanamine, α-methyl-N-(phenylmethyl)-, (αR)-, Benzyl((R)-1-phenylethyl)amine, N-Benzyl((R)-1-phenylethyl)amine, N-Benzyl-(R)-α-methylbenzylamine, N-Benzyl-1-phenylethanamine, N-[(R)-1-Phenylethyl]benzylamine, benzenemethanamine, alpha-methyl-N-(phenylmethyl)-
• CAS: 38235-77-7

Description

(R)-(+)-N-Benzyl-1-phenylethylamine is an enantiomer of phenylethylamine. It is a chiral, vinylic amine that can be used to produce catalytic asymmetric Grignard reactions. The synthesis of this compound starts with the addition of benzyl chloride to 1-phenylethylamine. This reaction produces (R)-(+)-N-benzyl-1-phenylethylamine as the major product and its corresponding bisulfate salt as the minor product. This compound has been shown to be an anti HIV drug in a number of studies, which may be due to its ability to inhibit reverse transcriptase and/or prevent viral entry into cells.

• Brand: Biosynth

Chemical properties

• Molecular weight: 211.3 g/mol
• Formula: C₁₅H₁₇N
• Purity: Min. 95%
• Color/Form: Colourless To Pale Yellow Liquid
• InChI: InChI=1S/C15H17N/c1-13(15-10-6-3-7-11-15)16-12-14-8-4-2-5-9-14/h2-11,13,16H,12H2,1H3/t13-/m1/s1
• InChI key: InChIKey=ZYZHMSJNPCYUTB-CYBMUJFWSA-N
• SMILES: C[C@@H](NCc1ccccc1)c1ccccc1