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1,2-Diiodo-4,5-di-n-octyloxybenzene

Base Information
  • Chemical Name:1,2-Diiodo-4,5-di-n-octyloxybenzene
  • CAS No.:248277-14-7
  • Molecular Formula:C22H36I2O2
  • Molecular Weight:586.336
  • Hs Code.:
  • Mol file:248277-14-7.mol
1,2-Diiodo-4,5-di-n-octyloxybenzene

Synonyms:1,2-Diiodo-4,5-dioctyloxybenzene

Suppliers and Price of 1,2-Diiodo-4,5-di-n-octyloxybenzene
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
  • Strem Chemicals
  • 1,2-Diiodo-4,5-di-n-octyloxybenzene
  • 1g
  • $ 385.00
  • Strem Chemicals
  • 1,2-Diiodo-4,5-di-n-octyloxybenzene
  • 250mg
  • $ 128.00
  • American Custom Chemicals Corporation
  • 1,2-DIOCTYLOXY-4,5-DIIODOBENZENE 95.00%
  • 5MG
  • $ 497.35
Total 7 raw suppliers
Chemical Property of 1,2-Diiodo-4,5-di-n-octyloxybenzene
Chemical Property:
  • Boiling Point:522.9±50.0 °C(Predicted) 
  • PSA:18.46000 
  • Density:1.420±0.06 g/cm3(Predicted) 
  • LogP:8.37440 
Purity/Quality:

97% *data from raw suppliers

1,2-Diiodo-4,5-di-n-octyloxybenzene *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 1,2-Diiodo-4,5-di-n-octyloxybenzene

There total 1 articles about 1,2-Diiodo-4,5-di-n-octyloxybenzene 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 sulfuric acid; iodine; acetic acid; periodic acid; In water; at 80 ℃; for 18h;
DOI:10.1039/c7ob01907f
Guidance literature:
Multi-step reaction with 3 steps
1.1: diisopropylamine; copper(l) iodide; tetrakis(triphenylphosphine) palladium(0) / Inert atmosphere
1.2: Inert atmosphere
2.1: diisopropylamine; copper(l) iodide; tetrakis(triphenylphosphine) palladium(0) / 48 h / 20 °C / Inert atmosphere
3.1: iodine / chloroform / 12 h / 20 °C / Inert atmosphere
With copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); iodine; diisopropylamine; In chloroform;
DOI:10.1021/ol5015366
Guidance literature:
1,2-diiodo-4,5-bis(octyloxy)benzene; trimethylsilylacetylene; With copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); diisopropylamine; Inert atmosphere;
With potassium hydroxide; In thionyl chloride; Inert atmosphere;
DOI:10.1021/ol5015366
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