156769-81-2

Basic information

• Product Name: Carbamic acid, (1-methyl-2-butenyl)-, 1,1-dimethylethyl ester, (E)- (9CI)
• Synonyms: Carbamic acid, (1-methyl-2-butenyl)-, 1,1-dimethylethyl ester, (E)- (9CI);tert-butyl N-[(E)-1-methylbut-2-enyl]carbamate
• CAS NO: 156769-81-2
• Molecular Formula: C10H19NO2
• Molecular Weight: 185.26336
• Product Categories: N-BOC
• Mol File: 156769-81-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 253.9±19.0 °C(Predicted)
• Appearance: /
• Density: 0.926±0.06 g/cm3(Predicted)
• PKA: 12.28±0.46(Predicted)
• CAS DataBase Reference: Carbamic acid, (1-methyl-2-butenyl)-, 1,1-dimethylethyl ester, (E)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, (1-methyl-2-butenyl)-, 1,1-dimethylethyl ester, (E)- (9CI)(156769-81-2)
• EPA Substance Registry System: Carbamic acid, (1-methyl-2-butenyl)-, 1,1-dimethylethyl ester, (E)- (9CI)(156769-81-2)

Safety Data

• Hazardous Substances Data: 156769-81-2(Hazardous Substances Data)

Downstream Products

• 161396-52-7 ((E)-1-Methyl-but-2-enyl)-[(toluene-4-sulfonylamino)-methyl]-carbamic acid tert-butyl ester 

Relevant articles and documents

Oxaziridine-mediated amination of branched allylic sulfides: Stereospecific formation of allylic amine derivatives via [2,3]-sigmatropic rearrangement

Reaction of branched allylic sulfides with the N-Bocoxaziridine 1 results in [2,3]-sigmatropic rearrangement of the intermediate allylic N-Boc-surfimides with a high level of chirality transfer. The first example of formation of a quaternary stereocenter