10-Bromo-1-decene

Suppliers

Names

[ CAS No. ]:
62871-09-4

[ Name ]:
10-Bromo-1-decene

[Synonym ]:
10-Bromo-1-decene
MFCD00078660
1-Decene, 10-bromo-
10-bromodec-1-ene

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
239.3±19.0 °C at 760 mmHg

[ Molecular Formula ]:
C10H19Br

[ Molecular Weight ]:
219.162

[ Flash Point ]:
102.5±9.5 °C

[ Exact Mass ]:
218.067001

[ LogP ]:
5.42

[ Vapour Pressure ]:
0.1±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.465

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 9-Decen-1-ol
  • 1,10-Dibromodecane
  • Methyltriphenylphosphonium bromide
  • 9-bromo-1-nonanal
  • 9-decenyl methanesulfonate
  • 11-chloro-1-undecene
  • 1,7-Dibromoheptane
  • Allyl(bromo)magnesium
  • 9-bromnonan-1-ol
  • 1,9-Nonanediol

DownStream

  • ethyl 4-dec-9-enoxybenzoate
  • 1-decene
  • Dodecane
  • 1,19-Eicosadiene
  • 1-Hexadecene
  • N-hexane
  • Decan-1-ol
  • 1-Bromodecane
  • 4-dec-9-enoxybenzoic acid
  • dodec-1-en-11-yne

Articles

Synthesis of gamma,delta-unsaturated-beta-keto lactones via sequential cross metathesis-lactonization: a facile entry to macrolide antibiotic (-)-A26771B.

J. Org. Chem. 71(5) , 2021-5, (2006)

A simple access to gamma,delta-unsaturated-beta-keto lactones is presented, allowing a rapid total synthesis of the naturally occurring 16-membered macrolide antibiotic (-)-A26771B via cross metathesi...

Novel ferroelectric and electroclinic organosiloxane liquid crystals. Naciri J, et al.

Chem. Mater. 7(7) , 1397-1402, (1995)

Radical initiation using borole derivatives. Montgomery I, et al.

Tetrahedron Lett. 49(4) , 628-630, (2008)


More Articles

Related Compounds

  • 10-bromo-1-(2-tetrahydropyranyloxy)-(Z)-decene
  • 10-bromo-1-(2-tetrahydropyranyloxy)-(E)-9-decene
  • 10-bromo-1-ethenylsulfonyldec-1-ene
  • 10-Bromo-1,1-diethoxydecane
  • 10-bromo-1,8-dichloroanthracene
  • 10-bromo-1,2,3,4,12,12a-hexahydro-6H-pyrazino[2,1-c][1,4]benzoxazepin-6-one hydrochloride
  • 1-(1-{[(Tert-butoxy)carbonyl]amino}-2,2-dimethylpropyl)-3-hydroxycyclobutane-1-carboxylic acid
  • Dimethyl({[2-(piperidin-4-yloxy)-1,3-thiazol-5-yl]methyl})amine
  • 3-Amino-2-(3-fluoro-2-methylphenyl)propan-1-ol
  • 2-(1-Isocyanatocyclopropyl)-1-benzothiophene
  • tert-butyl N-[1-(5-chloropyridin-2-yl)-2-oxoethyl]carbamate
  • 2-(1,5-dimethyl-1H-pyrazol-4-yl)butanedioic acid
  • N,N-dimethyl-5-(pyrrolidin-3-ylmethyl)-1,3-thiazol-2-amine
  • 6-chloro-3-(1H-imidazol-4-yl)-1-methyl-1H-indole
  • 1-[1-(Oxolan-2-yl)cyclopropyl]ethan-1-one
  • 2-{Imidazo[1,2-a]pyridin-3-yl}-2-methylpropanal
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