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5-Bromo-2-iodo-1,1'-biphenyl

Base Information
  • Chemical Name:5-Bromo-2-iodo-1,1'-biphenyl
  • CAS No.:4510-78-5
  • Molecular Formula:C12H8BrI
  • Molecular Weight:359.004
  • Hs Code.:2903999090
  • European Community (EC) Number:667-765-6
  • DSSTox Substance ID:DTXSID001309582
  • Mol file:4510-78-5.mol
5-Bromo-2-iodo-1,1'-biphenyl

Synonyms:5-Bromo-2-iodo-1,1'-biphenyl;4510-78-5;4-bromo-1-iodo-2-phenylbenzene;5-broMo-2-iodo-biphenyl;SCHEMBL16943347;3-bromo-6-iodo-1,1'-biphenyl;DTXSID001309582;AKOS024432683;E89392

Suppliers and Price of 5-Bromo-2-iodo-1,1'-biphenyl
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
  • 5-BROMO-2-IODOBIPHENYL Aldrich
  • 1ea
  • $ 57.00
  • American Custom Chemicals Corporation
  • 5-BROMO-2-IODOBIPHENYL 95.00%
  • 5MG
  • $ 500.95
Total 8 raw suppliers
Chemical Property of 5-Bromo-2-iodo-1,1'-biphenyl
Chemical Property:
  • PSA:0.00000 
  • LogP:4.72070 
  • XLogP3:4.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:1
  • Exact Mass:357.88541
  • Heavy Atom Count:14
  • Complexity:177
Purity/Quality:

98%, *data from raw suppliers

5-BROMO-2-IODOBIPHENYL Aldrich *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C2=C(C=CC(=C2)Br)I
Technology Process of 5-Bromo-2-iodo-1,1'-biphenyl

There total 4 articles about 5-Bromo-2-iodo-1,1'-biphenyl 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 toluene-4-sulfonic acid; potassium iodide; sodium nitrite; In acetonitrile; at 10 - 20 ℃; for 2h;
DOI:10.1002/anie.201309104
Guidance literature:
Multi-step reaction with 2 steps
1: ammonium bromide; acetic acid; dihydrogen peroxide / 20 °C / Schlenk technique
2: toluene-4-sulfonic acid; sodium nitrite; potassium iodide / acetonitrile / 2 h / 10 - 20 °C
With dihydrogen peroxide; toluene-4-sulfonic acid; ammonium bromide; acetic acid; potassium iodide; sodium nitrite; In acetonitrile;
DOI:10.1002/anie.201309104
Guidance literature:
With potassium iodide; Diazotization;
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