tert-butyl n,n-diallylcarbamate

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Names

[ CAS No. ]:
151259-38-0

[ 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)


More Articles

Related Compounds

  • 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
  • 2,3-Dimethyl-6-(1-methylcyclopropyl)imidazo[2,1-b][1,3]thiazole-5-sulfonyl fluoride
  • 6-Cyclopropyl-3-ethylimidazo[2,1-b][1,3]thiazole-5-sulfonyl fluoride
  • 6-Cyclobutyl-3-ethylimidazo[2,1-b][1,3]thiazole-5-sulfonyl fluoride
  • 2-{[(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]methyl}cyclohexane-1-carboxylic acid
  • 4-[5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanamido]cyclohexane-1-carboxylic acid
  • (2R)-2-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-methylpentanamido]-3,3-dimethylbutanoic acid
  • (3R)-1-{3-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]pentanoyl}piperidine-3-carboxylic acid
  • 3-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-1-methylcyclopentanecarbonyl]-1,3-thiazolidine-4-carboxylic acid
  • 3-({1-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]cyclopentyl}formamido)-2-methoxypropanoic acid
  • 1-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-phenylacetyl]pyrrolidine-3-carboxylic acid
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