167226-15-5

Basic information

• Product Name: [(S)-aziridin-2-yl](diphenyl)methanol
• Synonyms: [(S)-aziridin-2-yl](diphenyl)methanol
• CAS NO: 167226-15-5
• Molecular Weight: 225.29
• Mol File: 167226-15-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: [(S)-aziridin-2-yl](diphenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: [(S)-aziridin-2-yl](diphenyl)methanol(167226-15-5)
• EPA Substance Registry System: [(S)-aziridin-2-yl](diphenyl)methanol(167226-15-5)

Safety Data

• Hazardous Substances Data: 167226-15-5(Hazardous Substances Data)

Upstream product

• 108-86-1 bromobenzene 
• 75154-68-6 methyl (2S)-N-tritylaziridine-2-carboxylate 
• 167226-20-2 (S)-α,α-diphenyl-1-(triphenylmethyl)-2-aziridinemethanol 

Downstream Products

• 78603-91-5 (S)-2-amino-1,1-diphenylpropan-1-ol 
• 1221817-39-5 (S)-diphenyl[1-(2-nitrobenzenesulfonyl)aziridine-2-yl]methanol 
• 908293-62-9 (2S)-(1-tosylaziridin-2-yl)diphenylmethanol 

Relevant articles and documents

Direct asymmetric aldol reaction of 5H-oxazol-4-ones with aldehydes catalyzed by chiral guanidines

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Aziridin-2-yl methanols as organocatalysts in Diels-Alder reactions and Friedel-Crafts alkylations of N-methyl-pyrrole and N-methyl-indole

A series of enantiomerically pure aziridin-2-yl methanols have been synthesized from aziridine-2-carboxylic esters and have been tested as organocatalysts in Diels-Alder reactions and Friedel-Crafts alkylations of N-methyl-pyrrole and N-methyl-indole usin

Asymmetric Ketone Reduction using Chiral Oxazaborolidines derived from Aziridine Carbinols

Asymmetric borane reduction of acetophenone using 1,3,2-oxazaborolidines derived from aziridine-2-tertiary alcohols 1 and 2 yielded the corresponding alcohol in high optical yields.The synthesis of the novel chiral catalysts 1 and 2 using D-and L-serine,