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4,6-Dichloroisophthaloyl dichloride

Base Information Edit
  • Chemical Name:4,6-Dichloroisophthaloyl dichloride
  • CAS No.:2855-01-8
  • Molecular Formula:C8H2Cl4O2
  • Molecular Weight:271.91200
  • Hs Code.:
  • Mol file:2855-01-8.mol
4,6-Dichloroisophthaloyl dichloride

Synonyms:4,6-dichloro-isophthaloyl chloride;4,6-Dichlor-isophthaloylchlorid;4,6-Dichlor-isophthalsaeure-dichlorid;4.6-Dichlor-isophthalsaeuredichlorid;4,6-Dichlorisophthalsaeure-dichlorid;

Suppliers and Price of 4,6-Dichloroisophthaloyl dichloride
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
Total 1 raw suppliers
Chemical Property of 4,6-Dichloroisophthaloyl dichloride Edit
Chemical Property:
  • PSA:34.14000 
  • LogP:3.75140 
Purity/Quality:

95% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 4,6-Dichloroisophthaloyl dichloride

There total 6 articles about 4,6-Dichloroisophthaloyl dichloride 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 phosphorus pentachloride; In tetrachloromethane; for 4h; Heating;
DOI:10.1039/a606932k
Guidance literature:
With thionyl chloride; at 240 ℃; im Rohr;
Guidance literature:
Multi-step reaction with 2 steps
1: 38 percent / conc. HNO3 (d=1.4) / nitrobenzene / 30 h / 150 - 180 °C
2: 86 percent / PCl5 / CCl4 / 4 h / Heating
With phosphorus pentachloride; nitric acid; In tetrachloromethane; nitrobenzene;
DOI:10.1039/a606932k
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