10-Bromo-1-decene

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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
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • Dehydroanonaine
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2,2-Dimethylpiperidine-3-carboxylic acid
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • L-Norvalinamide, L-alanyl-
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  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 1-[(3-Chlorophenyl)amino]-4,5-dihydroxy-8-nitro-9,10-anthracenedione