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4-(bromomethyl)-1-chloro-2-iodobenzene

Base Information
  • Chemical Name:4-(bromomethyl)-1-chloro-2-iodobenzene
  • CAS No.:136558-15-1
  • Molecular Formula:C7H5BrClI
  • Molecular Weight:331.378
  • Hs Code.:2903998090
4-(bromomethyl)-1-chloro-2-iodobenzene

Synonyms:4-(bromomethyl)-1-chloro-2-iodobenzene

Suppliers and Price of 4-(bromomethyl)-1-chloro-2-iodobenzene
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
  • TRC
  • 4-(Bromomethyl)-1-chloro-2-iodo-Benzene
  • 100mg
  • $ 220.00
  • TRC
  • 4-(Bromomethyl)-1-chloro-2-iodo-Benzene
  • 50mg
  • $ 130.00
  • Labseeker
  • 4-(bromomethyl)-1-chloro-2-iodobenzene 95
  • 2g
  • $ 1083.00
  • American Custom Chemicals Corporation
  • 4-(BROMOMETHYL)-1-CHLORO-2-IODOBENZENE 95.00%
  • 5MG
  • $ 496.64
  • Alichem
  • 4-Chloro-3-iodobenzylbromide
  • 1g
  • $ 1519.80
  • Alichem
  • 4-Chloro-3-iodobenzylbromide
  • 500mg
  • $ 847.60
  • Advanced Chemicals Intermediatesced Chemicals Intermediates
  • 4-Bromomethyl-1-chloro-2-iodo-benzene 95%+
  • 1g
  • $ 572.75
  • Advanced Chemicals Intermediatesced Chemicals Intermediates
  • 4-Bromomethyl-1-chloro-2-iodo-benzene 95%+
  • 5g
  • $ 1732.75
  • Acints
  • 4-Bromomethyl-1-chloro-2-iodo-benzene 95%+
  • 5g
  • $ 1732.75
  • Acints
  • 4-Bromomethyl-1-chloro-2-iodo-benzene 95%+
  • 1g
  • $ 572.75
Total 0 raw suppliers
Chemical Property of 4-(bromomethyl)-1-chloro-2-iodobenzene
Chemical Property:
Purity/Quality:

4-(Bromomethyl)-1-chloro-2-iodo-Benzene *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 4-(bromomethyl)-1-chloro-2-iodobenzene

There total 4 articles about 4-(bromomethyl)-1-chloro-2-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 carbon tetrabromide; triphenylphosphine; In dichloromethane; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.1021/acs.jmedchem.1c00110
Guidance literature:
Multi-step reaction with 2 steps
1: sodium tetrahydroborate / methanol / 2 h / 20 °C / Inert atmosphere
2: carbon tetrabromide; triphenylphosphine / dichloromethane / 2 h / 20 °C / Inert atmosphere
With sodium tetrahydroborate; carbon tetrabromide; triphenylphosphine; In methanol; dichloromethane;
DOI:10.1021/acs.jmedchem.1c00110
Guidance literature:
Multi-step reaction with 3 steps
1: iodine; sodium iodate; sulfuric acid / water / 1 h / 20 °C / Inert atmosphere
2: sodium tetrahydroborate / methanol / 2 h / 20 °C / Inert atmosphere
3: carbon tetrabromide; triphenylphosphine / dichloromethane / 2 h / 20 °C / Inert atmosphere
With sodium tetrahydroborate; sodium iodate; carbon tetrabromide; sulfuric acid; iodine; triphenylphosphine; In methanol; dichloromethane; water;
DOI:10.1021/acs.jmedchem.1c00110
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