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1,4-Dibromocyclohexane

Base Information
  • Chemical Name:1,4-Dibromocyclohexane
  • CAS No.:35076-92-7
  • Molecular Formula:C6H10 Br2
  • Molecular Weight:241.953
  • Hs Code.:2903890090
  • European Community (EC) Number:252-349-5
  • NSC Number:16622
  • DSSTox Substance ID:DTXSID6067888
  • Nikkaji Number:J61.217K,J61.218I,J88.988A
  • Mol file:35076-92-7.mol
1,4-Dibromocyclohexane

Synonyms:1,4-DIBROMOCYCLOHEXANE;35076-92-7;13618-83-2;Cyclohexane, 1,4-dibromo-;TRANS-1,4-DIBROMOCYCLOHEXANE;1beta,4alpha-Dibromocyclohexane;Cyclohexane, 1,4-dibromo-, trans-;EINECS 252-349-5;1,4-dibromo-cyclohexane;NSC16622;16661-99-7;1alpha,4beta-Dibromocyclohexane;SCHEMBL3212874;SCHEMBL9170897;1alpha,4alpha-Dibromocyclohexane;DTXSID6067888;SCHEMBL16919059;AMY6604;MFCD00014281;NSC-16622;AKOS028109238;FT-0639228;A1-24391

Suppliers and Price of 1,4-Dibromocyclohexane
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
Total 7 raw suppliers
Chemical Property of 1,4-Dibromocyclohexane
Chemical Property:
  • Vapor Pressure:0.133mmHg at 25°C 
  • Boiling Point:224.9°Cat760mmHg 
  • Flash Point:95.1°C 
  • PSA:0.00000 
  • Density:1.789g/cm3 
  • LogP:3.08740 
  • XLogP3:3.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:241.91288
  • Heavy Atom Count:8
  • Complexity:54.9
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CC(CCC1Br)Br
Technology Process of 1,4-Dibromocyclohexane

There total 9 articles about 1,4-Dibromocyclohexane 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 hydrogen; In tetrahydrofuran; at 20 ℃; for 8h; under 760.051 Torr;
DOI:10.1016/j.tetlet.2011.02.083
Guidance literature:
Multi-step reaction with 3 steps
1: concentrated sulfuric acid
3: HBr
With sulfuric acid; hydrogen bromide;
Guidance literature:
Multi-step reaction with 2 steps
2: HBr
With hydrogen bromide;
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