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1-Bromo-4-iodobenzene

Base Information Edit
  • Chemical Name:1-Bromo-4-iodobenzene
  • CAS No.:589-87-7
  • Molecular Formula:C6H4BrI
  • Molecular Weight:282.906
  • Hs Code.:29036990
  • European Community (EC) Number:209-662-7
  • NSC Number:8033
  • UNII:R9LDG2XS7C
  • DSSTox Substance ID:DTXSID5060433
  • Nikkaji Number:J94.975B
  • Wikidata:Q72457473
  • Mol file:589-87-7.mol
1-Bromo-4-iodobenzene

Synonyms:1-Bromo-4-iodobenzene;589-87-7;4-BROMOIODOBENZENE;p-Bromoiodobenzene;Benzene, 1-bromo-4-iodo-;p-Iodobromobenzene;4-bromo-1-iodobenzene;p-Bromophenyl iodide;4-iodobromobenzene;1-bromo-4-iodo-benzene;MFCD00001051;4-bromophenyl iodide;4-iodo-1-bromobenzene;1-Bromo-4-iodobenzene-[13C6];R9LDG2XS7C;NSC 8033;NSC-8033;EINECS 209-662-7;AI3-09032;NSC8033;p-bromo iodobenzene;4-bromo iodobenzene;4-bromo-iodobenzene;4-iodo bromobenzene;4-iodo-bromobenzene;para-bromoiodobenzene;4-bromo-iodo-benzene;1-bromo-4-iodobezene;1-Iodo-4-Brombenzene;1-iodo-4-bromobenzene;1-bromo-4-iodo benzene;1-iodo-4-bromo-benzene;4-bromo-1-iodo-benzene;UNII-R9LDG2XS7C;SCHEMBL24146;1-bromanyl-4-iodanyl-benzene;1-Bromo-4-iodobenzene, 98%;DTXSID5060433;AC-174;1-BROMO-4-IODO(?H?)BENZENE;AKOS000185502;CS-W008977;GS-3007;OL10130;BP-13428;SY005124;A8313;AM20040789;B0604;BB 0268019;FT-0617892;EN300-71276;A832097;J-504447;Z299596184

Suppliers and Price of 1-Bromo-4-iodobenzene
Supply Marketing:Edit
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
  • TRC
  • 1-Bromo-4-iodobenzene
  • 5g
  • $ 55.00
  • TCI Chemical
  • 1-Bromo-4-iodobenzene
  • 25G
  • $ 67.00
  • TCI Chemical
  • 1-Bromo-4-iodobenzene
  • 250G
  • $ 405.00
  • Sigma-Aldrich
  • 1-Bromo-4-iodobenzene 98%
  • 25g
  • $ 155.00
  • Sigma-Aldrich
  • 1-Bromo-4-iodobenzene 98%
  • 5g
  • $ 48.50
  • Oakwood
  • 1-Bromo-4-iodobenzene
  • 25g
  • $ 18.00
  • Oakwood
  • 1-Bromo-4-iodobenzene
  • 10g
  • $ 14.00
  • Oakwood
  • 1-Bromo-4-iodobenzene
  • 5g
  • $ 12.00
  • Oakwood
  • 1-Bromo-4-iodobenzene
  • 1g
  • $ 10.00
  • Oakwood
  • 1-Bromo-4-iodobenzene
  • 100g
  • $ 48.00
Total 183 raw suppliers
Chemical Property of 1-Bromo-4-iodobenzene Edit
Chemical Property:
  • Appearance/Colour:white to brown cryst. powder, crystals or needles 
  • Vapor Pressure:0.0464mmHg at 25°C 
  • Melting Point:89-91 °C(lit.) 
  • Refractive Index:1.654 
  • Boiling Point:244.8 °C at 760 mmHg 
  • Flash Point:101.9 °C 
  • PSA:0.00000 
  • Density:2.215 g/cm3 
  • LogP:3.05370 
  • Storage Temp.:Store below +30°C. 
  • Sensitive.:Light Sensitive 
  • Solubility.:0.008g/l 
  • Water Solubility.:Insoluble in water. 
  • XLogP3:4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:281.85411
  • Heavy Atom Count:8
  • Complexity:66.9
Purity/Quality:

99% *data from raw suppliers

1-Bromo-4-iodobenzene *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36-37/39 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:Other Classes -> Halogenated Monoaromatics
  • Canonical SMILES:C1=CC(=CC=C1Br)I
  • Uses 1. 1-Bromo-4-iodobenzene is used for organic synthesis. 2. Used as substrate for copper-free Sonogashira coupling reaction in aqueous acetone. 3. For the synthesis of β,β-dibromostyrene. suzuki reaction 1-Bromo-4-iodobenzene has been employed:as reagent for in situ desilylation and coupling of silylated alkynesas starting reagent in the total syntheses of ent-conduramine A and ent-7-deoxypancratistatin (alkaloids)as substrate in copper-free Sonogashira coupling in aqueous acetone in synthesis of β,β,dibromostyrenes
Technology Process of 1-Bromo-4-iodobenzene

There total 83 articles about 1-Bromo-4-iodobenzene 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 potassium iodide; In water; at 25 ℃; for 0.0833333h; Solvent;
DOI:10.2174/1570178614666170907120329
Guidance literature:
With N-Bromosuccinimide; In N,N-dimethyl-formamide; at 20 ℃; for 4h;
DOI:10.1002/anie.202008372
Guidance literature:
With N-iodo-succinimide; In N,N-dimethyl-formamide; at 50 ℃; for 4h;
DOI:10.1002/anie.202008372
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