158149-99-6

Basic information

• Product Name: L-2-AMINOMETHYLPHE
• Synonyms: L-2-AMINOMETHYLPHE;L-2-AMINOMETHYLPHENYLALANINE;L-2-Aminomethylphenylalanine≥ 99% (HPLC)
• CAS NO: 158149-99-6
• Molecular Formula: C₁₀H₁₄N₂O₂
• Molecular Weight: 194.23
• Product Categories: Phenylalanine analogs and other aromatic alpha amino acids
• Mol File: 158149-99-6.mol
• Article Data: 3

Chemical Properties

• Melting Point: 224-225 °C
• Boiling Point: 377.5±42.0 °C(Predicted)
• Appearance: /
• Density: 1.234±0.06 g/cm3(Predicted)
• PKA: 0.92±0.10(Predicted)
• CAS DataBase Reference: L-2-AMINOMETHYLPHE(CAS DataBase Reference)
• NIST Chemistry Reference: L-2-AMINOMETHYLPHE(158149-99-6)
• EPA Substance Registry System: L-2-AMINOMETHYLPHE(158149-99-6)

Safety Data

• Hazardous Substances Data: 158149-99-6(Hazardous Substances Data)

Usage

Chemical Properties

White to off-white powder

Upstream product

• 158149-97-4 (2S)-(1S,2R,4R)-10-dicyclohexylsulfamoylisobornyl 2-amino-2-cyano-3-phenylpropanoate 
• 158149-98-5 (S)-2-Amino-2-aminomethyl-3-phenyl-propionic acid (1S,2R,4R)-1-[(dicyclohexylsulfamoyl)-methyl]-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester 

Relevant articles and documents

Highly enantioselective synthesis of (S)-α-alkyl-α,β- diaminopropionic acids via asymmetric phase-transfer catalytic alkylation of 2-phenyl-2-imidazoline-4-carboxylic acid tert-butyl esters

Image Presented An efficient enantioselective synthetic method for (S)-α-alkyl-α,β-diaminopropionic acid is reported. The asymmetric phase-transfer catalytic alkylation of N(1)-Boc-2-phenyl-2- imidazoline-4-carboxylic acid tert -butyl ester in the presenc

Stereoselective Amination of Chiral Enolates: Synthesis of Chiral Key Intermediates for β-Lactam Antibiotics

Stereoselective enolate trapping of lithium (1S,2R,4R)-1O-dicyclohexylsulfamoylisobornyl-2-cyano-3-phenylpropanoate with O-(diphenylphosphinyl)hydroxylamine followed by appropriate reduction, hydrolysis, and cyclisation processes allows the asymmetric syn