tert-butyl n,n-diallylcarbamate

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Names

[ Name ]:
tert-butyl n,n-diallylcarbamate

[Synonym ]:
diallylcarbamic acid tert-butyl ester
MFCD01321306
tert-Butyl N,N-diallylcarbamate
N-tert-butyloxycarbonyl-diallylamine
N-Boc-Diallylamine
N-(tert-butoxycarbonyl)diallylamine
tert-Butyl diallylcarbamate

Chemical & Physical Properties

[ Density]:
0.934g/cm3

[ Boiling Point ]:
242.7ºC at 760mmHg

[ Molecular Formula ]:
C₁₁H₁₉NO₂

[ Molecular Weight ]:
197.27400

[ Flash Point ]:
100.6ºC

[ Exact Mass ]:
197.14200

[ PSA ]:
29.54000

[ LogP ]:
2.59550

[ Vapour Pressure ]:
0.0334mmHg at 25°C

[ Index of Refraction ]:
n20/D 1.442(lit.)

[ Storage condition ]:
2-8°C

MSDS

Click to get detail MSDS

Safety Information

[ Hazard Codes ]:
Xi

[ HS Code ]:
2924199090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

Di-tert-butyl dicarbonate
Diallylamine

DownStream

(S)-1-(tert-Butoxycarbonyl)-2,5-dihydro-1H-pyrrole-2-carboxylic acid
N-Boc-3-pyrroline
3-Boc-6-oxa-3-aza-bicyclo[3.1.0]hexane

Customs

[ HS Code ]: 2924199090

[ Summary ]:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Hoveyda-Grubbs type metathesis catalyst immobilized on mesoporous molecular sieves MCM-41 and SBA-15.

Beilstein J. Org. Chem. 7 , 22-8, (2011)

A commercially available Hoveyda-Grubbs type catalyst (RC303 Zhannan Pharma) was immobilized on mesoporous molecular sieves MCM-41 and on SBA-15 by direct interaction with the sieve wall surface. The ...

Copper-Catalyzed Synthesis of 1, 2-Disubstituted Cyclopentanes from 1, 6-Dienes by Ring-Closing Kharasch Addition of Carbon Tetrachloride. Muñoz-Molina JM, et al.

Adv. Synth. Catal. 350(14-15) , 2365-2372, (2008)

tert-butyl N,N-diallylcarbamate
tert-butyl N,N-bis(tert-butyloxycarbonyl)-L-homoserinate
tert-butyl N,N-dibromocarbamate
tert-butyl N,N-bis(2-hydroxyethyl)carbamate
tert-butyl N,N-dibenzylcarbamate
tert-butyl N,N-di(propan-2-yl)carbamimidate
6-(Difluoromethyl)-3-methoxy-5-(trifluoromethoxy)pyridin-2-amine
4-(Difluoromethyl)-6-iodo-3-(trifluoromethyl)picolinonitrile
2-Chloro-4-(difluoromethyl)-5-nitro-3-(trifluoromethoxy)pyridine
2-Bromo-4-(bromomethyl)-6-(difluoromethyl)-3-iodopyridine
2-Chloro-5-(difluoromethyl)-4-(trifluoromethoxy)nicotinonitrile
2-Chloro-5-(difluoromethyl)-6-methoxy-3-(trifluoromethoxy)pyridine
2-Bromo-6-(difluoromethyl)-5-methylnicotinamide
2-(2-Cyano-4-(difluoromethoxy)-5-(hydroxymethyl)phenyl)acetic acid
2-Amino-4-(difluoromethyl)-5-methylnicotinamide
2-Chloro-5-(difluoromethyl)-3-methylisonicotinamide

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