ChemicalBook Product Catalog Chemical Reagents Organic reagents Esters Other esters TERT-BUTYL N-ALLYLCARBAMATE

TERT-BUTYL N-ALLYLCARBAMATE

TERT-BUTYL N-ALLYLCARBAMATE Basic information
Product Name:TERT-BUTYL N-ALLYLCARBAMATE
Synonyms:ALLYL-CARBAMIC ACID TERT-BUTYL ESTER;TERT-BUTYL N-ALLYLCARBAMATE;N-ALLYL-T-BUTYLCARBAMATE;3-(tert-Butoxycarbonylamino)-1-propene;N-(tert-Butyloxycarbonyl)-2-propene-1-amine;N-Allylcarbamic acid tert-butyl ester;tert-Butoxycarbonylallylamine;tert-Butyl allylcarbamate
CAS:78888-18-3
MF:C8H15NO2
MW:157.21
EINECS:
Product Categories:N-BOC;Allyl Monomers;Monomers;Polymer Science
Mol File:78888-18-3.mol
TERT-BUTYL N-ALLYLCARBAMATE Structure
TERT-BUTYL N-ALLYLCARBAMATE Chemical Properties
Melting point 36-38 °C (lit.)
Boiling point 48-50°C/0.3mm
density 0.938 g/mL at 25 °C (lit.)
refractive index 1.4720 (estimate)
Fp 175 °F
storage temp. Inert atmosphere,Room Temperature
pka12.60±0.46(Predicted)
form Low Melting Solid
color Colorless
Water Solubility Insoluble in water. Soluble in methanol.
Safety Information
Hazard Codes Xi,Xn
Risk Statements 22-36/37/38
Safety Statements 22-26-36/37/39
RIDADR UN 1325 4.1/PG 2
WGK Germany 3
HazardClass IRRITANT
HS Code 29241990
MSDS Information
ProviderLanguage
SigmaAldrich English
TERT-BUTYL N-ALLYLCARBAMATE Usage And Synthesis
Chemical Propertieswhite solid crystalline
Usestert-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 .
TERT-BUTYL N-ALLYLCARBAMATE Preparation Products And Raw materials
Preparation Productstert-butyl azidoformate-->N-BOC PRROLIDIN-2-OL-->N-T-BOC-PYRROLE
2-OXO-2,5-DIHYDRO-PYRROLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER BOC-1,2,5,6-TETRAHYDROPYRIDINE-4-CARBOXYLIC ACID (S)-4-METHYLENE-PYRROLIDINE-1,2-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER N-Boc-pyrroline (-)-(1S,4R)-N-BOC-4-AMINOCYCLOPENT-2-ENECARBOXYLIC ACID N-Boc-1,2,5,6-tetrahydropyridine-4-boronic acid pinacol ester TERT-BUTYL N,N-DIALLYLCARBAMATE N-Boc-3,4-dehydro-D-proline Methyl N-Boc-L-proline-3-ene 1(2H)-Pyridinecarboxylic acid, 3,6-dihydro-5-((methoxyimino)methyl)-, 1,1-dimethylethyl ester, (E)- BOC-2,5-DIHYDRO-D-PHENYLGLYCINE 3-ALLYL-4-HYDROXY-4,5-DIMETHYL-5-(4-METHYL-3-PENTENYL)-1,3-OXAZOLIDIN-2-ONE CARBAMIC ACID, [4(S)-(HYDROXYMETHYL)-2-CYCLOPENTEN-1-YL]-1,1-DIMETHYLETHYL ESTER, (1R-CIS)- TERT-BUTYL N-ALLYLCARBAMATE (R)-2-TERT-BUTOXYCARBONYLAMINO-3-METHYL-BUT-3-ENOIC ACID BOC-1,2,5,6-TETRAHYDROPYRIDINE-3-CARBOXYLIC ACID BOC-3,4-DEHYDRO-PRO-OH BOC-5-AMINO-1,3-CYCLOHEXADIENE-1-CARBOXYLIC ACID
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