1401003-93-7

Basic information

• Product Name: tert-butyl (2-hydroxy-2-phenylpropyl)carbamate
• Synonyms: tert-butyl (2-hydroxy-2-phenylpropyl)carbamate
• CAS NO: 1401003-93-7
• Molecular Weight: 251.326
• Mol File: 1401003-93-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: tert-butyl (2-hydroxy-2-phenylpropyl)carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (2-hydroxy-2-phenylpropyl)carbamate(1401003-93-7)
• EPA Substance Registry System: tert-butyl (2-hydroxy-2-phenylpropyl)carbamate(1401003-93-7)

Safety Data

• Hazardous Substances Data: 1401003-93-7(Hazardous Substances Data)

Upstream product

• 17643-24-2 (+/-)-1-amino-2-phenylpropan-2-ol 
• 24424-99-5 di-tert-butyl dicarbonate 
• 98-83-9 isopropenylbenzene 
• 36016-38-3 tert-Butyl N-hydroxycarbamate 
• 105838-14-0 tert-butyl N-tosyloxycarbamate 

Relevant articles and documents

Nitration-Peroxidation of Alkenes: A Selective Approach to β-Peroxyl Nitroalkanes

Nitration-peroxidation of alkenes for the synthesis of β-peroxyl nitroalkanes has been developed by using tert-butyl nitrite and tert-butyl hydroperoxide. The method presents a new and selective difunctionalization of alkenes to introduce a nitro group and a peroxyl group across the double bonds of alkenes under mild conditions. A radical reaction pathway is proposed by experimental and theoretical studies.

Osmium-catalyzed vicinal oxyamination of alkenes by N-(4- toluenesulfonyloxy)carbamates

N-(4-Toluenesulfonyloxy)carbamates based on a range of common amine protecting groups serve as preformed nitrogen sources in the intermolecular osmium-catalyzed oxyamination reaction of a variety of mono-, di-, and trisubstituted alkenes. The reactions occur with low catalyst loadings and good yields and afford high regioselectivity for unsymmetrically substituted alkenes.