860312-72-7

Basic information

• Product Name: tert-butyl (3-hydroxy-3-methyl-1-phenylbutan-2-yl)carbamate
• Synonyms: tert-butyl (3-hydroxy-3-methyl-1-phenylbutan-2-yl)carbamate
• CAS NO: 860312-72-7
• Molecular Weight: 279.379
• Mol File: 860312-72-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tert-butyl (3-hydroxy-3-methyl-1-phenylbutan-2-yl)carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (3-hydroxy-3-methyl-1-phenylbutan-2-yl)carbamate(860312-72-7)
• EPA Substance Registry System: tert-butyl (3-hydroxy-3-methyl-1-phenylbutan-2-yl)carbamate(860312-72-7)

Safety Data

• Hazardous Substances Data: 860312-72-7(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 144899-38-7 DL-3-Amino-2-methyl-4-phenyl-2-butanol 
• 5619-07-8 methyl 2-amino-3-phenylpropanoate hydrochloride 
• 150-30-1 Phenylalanine 
• 75-16-1 methylmagnesium bromide 
• 860312-99-8 1-(N-tert.-butyloxycarbonyl-amino)-2-(S)-phenylethyl methyl ketone 

Downstream Products

• 352438-06-3 4-benzyl-5,5-dimethyloxazolidin-2-one 
• 860312-71-6 3-amino-2-methyl-4-phenylbutan-2-ol hydrochloride 

Relevant articles and documents

Controllable Intramolecular Unactivated C(sp3)-H Amination and Oxygenation of Carbamates

Dual catalyst-controlled intramolecular unactivated C(sp3)-H amination and oxygenation of carbamates merging visible-light photocatalysis and earth-abundant transition metal catalysis have been reported. Useful amino alcohol and diol derivatives could be selectively obtained from readily available tertiary alcohol derivatives. The possible mechanisms have been proposed via a 1,5-HAT process followed by Lewis acid-controlled cyclization. The nickel and zinc catalysts inhibit the formation of oxygenation and amination products, respectively. An interesting phenomenon of chirality transfer is also observed.