1245623-78-2

Basic information

• Product Name: Benzeneethanol, β-aMino-3-chloro-, hydrochloride (1:1), (βR)-
• Synonyms: Benzeneethanol, β-aMino-3-chloro-, hydrochloride (1:1), (βR)-;(R)-2-AMINO-2-(3-CHLOROPHENYL)ETHANOL HYDROCHLORIDE;(R)-2-Amino-2-(3-chlorophenyl)ethan-1-ol hydrochloride
• CAS NO: 1245623-78-2
• Molecular Formula: C8H11Cl2NO
• Molecular Weight: 208.08504
• Mol File: 1245623-78-2.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: Benzeneethanol, β-aMino-3-chloro-, hydrochloride (1:1), (βR)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneethanol, β-aMino-3-chloro-, hydrochloride (1:1), (βR)-(1245623-78-2)
• EPA Substance Registry System: Benzeneethanol, β-aMino-3-chloro-, hydrochloride (1:1), (βR)-(1245623-78-2)

Safety Data

• Hazardous Substances Data: 1245623-78-2(Hazardous Substances Data)

Relevant articles and documents

Direct α-Imination of N-Acyl Pyrazoles with Nitrosoarenes

Unprecedented α-imino N-acyl pyrazoles were efficiently and selectively prepared through the 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD)-catalyzed reaction of nitrosoarenes with N-acyl pyrazoles via an N-nitroso aldol reaction/dehydration sequence. The α-imino acyl pyrazoles were demonstrated to be new versatile intermediates for practical one-pot syntheses of α-imino amides, dipeptide precursors, esters, and β-amino alcohols. The synthetic method competes with known protocols in terms of ready availability of the reagents and catalyst, mild and catalytic reaction conditions, gram-scale applicability, and scope of the α-imino acid derivatives achievable.