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2,6-Dibromo-1-hexene

Base Information
  • Chemical Name:2,6-Dibromo-1-hexene
  • CAS No.:87280-36-2
  • Molecular Formula:C6H10Br2
  • Molecular Weight:241.95200
  • Hs Code.:2903399090
  • European Community (EC) Number:662-219-3
  • DSSTox Substance ID:DTXSID70400932
  • Nikkaji Number:J2.411.665D
  • Wikidata:Q82204003
2,6-Dibromo-1-hexene

Synonyms:2,6-Dibromo-1-hexene;1-Hexene, 2,6-dibromo-;87280-36-2;DTXSID70400932;AKOS024339869

Suppliers and Price of 2,6-Dibromo-1-hexene
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Sigma-Aldrich
  • 2,6-DIBROMO-1-HEXENE Aldrich
  • 50mg
  • $ 57.00
  • American Custom Chemicals Corporation
  • 2,6-DIBROMO-1-HEXENE 95.00%
  • 5MG
  • $ 499.69
Total 0 raw suppliers
Chemical Property of 2,6-Dibromo-1-hexene
Chemical Property:
  • PSA:0.00000 
  • LogP:3.46020 
  • XLogP3:3.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:4
  • Exact Mass:241.91288
  • Heavy Atom Count:8
  • Complexity:68.9
Purity/Quality:

2,6-DIBROMO-1-HEXENE Aldrich *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C=C(CCCCBr)Br
Technology Process of 2,6-Dibromo-1-hexene

There total 5 articles about 2,6-Dibromo-1-hexene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With phosphorus tribromide; In pyridine; at 0 ℃; for 1h;
DOI:10.1021/jo00170a005
Guidance literature:
5,6-dibromohexan-1-ol; With potassium hydroxide; In diethyl ether; Heating;
methanesulfonyl chloride; With triethylamine; In dichloromethane; at 20 ℃;
With lithium bromide; In 1-methyl-pyrrolidin-2-one; at 20 ℃; Title compound not separated from byproducts;
DOI:10.1016/j.jorganchem.2006.08.061
Guidance literature:
Multi-step reaction with 2 steps
1.1: bromine / diethyl ether / 20 °C
2.1: potassium hydroxide / diethyl ether / Heating
2.2: NEt3 / CH2Cl2 / 20 °C
2.3: LiBr / 1-methyl-pyrrolidin-2-one / 20 °C
With potassium hydroxide; bromine; In diethyl ether;
DOI:10.1016/j.jorganchem.2006.08.061
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