CAS 78888-18-3
:N-allylcarbamate de tert-butyle
- Tert-Butyl Prop-2-En-1-Ylcarbamate
tert-Butyl N-allylcarbamate, 97%
CAS :tert-Butyl N-allylcarbamate is used in the synthesis of isoxazolidines. Synthesis of 5-substituted thiazolidin-2-ones is from the reaction of xanthates and tert-butyl N-allylcarbamates . This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some docu
Formule :C8H15NO2Degré de pureté :97%Couleur et forme :White to cream to pale yellow, Crystals or powder or crystalline powder or fused/lumpy solidMasse moléculaire :157.21Tert-butyl allylcarbamate
CAS :Formule :C8H15NO2Degré de pureté :96%Couleur et forme :SolidMasse moléculaire :157.2102tert-Butyl allylcarbamate
CAS :tert-Butyl allylcarbamateDegré de pureté :97%Masse moléculaire :157.21g/moltert-Butyl N-Allylcarbamate
CAS :Formule :C8H15NO2Degré de pureté :>98.0%(GC)Couleur et forme :White to Light yellow powder to lumpMasse moléculaire :157.21tert-Butyl allylcarbamate
CAS :Formule :C8H15NO2Degré de pureté :96%Couleur et forme :Solid, White powderMasse moléculaire :157.213tert-Butyl allylcarbamate
CAS :Tert-Butyl allylcarbamate is a fluorinated, reactive compound that has been used in the synthesis of amines and phosphazenes. Tert-Butyl allylcarbamate is an intermediate for the synthesis of isophthalaldehyde, which can be used to produce polymers and other organic compounds. The reaction rate of tert-butyl allylcarbamate is inhibited by phosphazene, which also inhibits polymerization. Tert-Butyl allylcarbamate has been shown to inhibit transfer reactions involving functional groups such as allylamine, silicon, and fluoroalkyl.
Formule :C8H15NO2Degré de pureté :Min. 95%Masse moléculaire :157.21 g/mol





