1012798-24-1

Basic information

• Product Name: (1r,4r)-4-((tert-butoxycarbonyl)amino)cyclohexyl benzoate
• Synonyms: (1r,4r)-4-((tert-butoxycarbonyl)amino)cyclohexyl benzoate
• CAS NO: 1012798-24-1
• Molecular Weight: 319.401
• Mol File: 1012798-24-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (1r,4r)-4-((tert-butoxycarbonyl)amino)cyclohexyl benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: (1r,4r)-4-((tert-butoxycarbonyl)amino)cyclohexyl benzoate(1012798-24-1)
• EPA Substance Registry System: (1r,4r)-4-((tert-butoxycarbonyl)amino)cyclohexyl benzoate(1012798-24-1)

Safety Data

• Hazardous Substances Data: 1012798-24-1(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 24424-99-5 di-tert-butyl dicarbonate 
• 1579-72-2 2,2,2-trifluoroethyl benzoate 
• 27489-62-9 trans-4-hydroxycyclohexylamine 
• 93-58-3 benzoic acid methyl ester 

Relevant articles and documents

μ-Oxo-Dinuclear-Iron(III)-Catalyzed O-Selective Acylation of Aliphatic and Aromatic Amino Alcohols and Transesterification of Tertiary Alcohols

A highly chemoselective and reactive μ-oxo-dinuclear iron(III) salen catalyst for transesterification was developed. The developed iron complex catalyzed acylation of aliphatic amino alcohols with nearly perfect O-selectivity, even when using activated esters, for which chemoselectivity is more difficult to control. In addition, O-selective transesterification of aromatic amino alcohols was achieved for the first time. The high activity of the iron complex enabled the use of sterically congested tertiary alcohols, including unprecedented tert-butanol.