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2,6-Dibromoterephthalic acid

Base Information
  • Chemical Name:2,6-Dibromoterephthalic acid
  • CAS No.:22191-58-8
  • Molecular Formula:C8H4Br2O4
  • Molecular Weight:323.925
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30596603
  • Nikkaji Number:J83.156E
  • Wikidata:Q82491904
  • Mol file:22191-58-8.mol
2,6-Dibromoterephthalic acid

Synonyms:2,6-Dibromoterephthalic acid;22191-58-8;SCHEMBL5560892;DTXSID30596603;JQJBHBWYLZTGAL-UHFFFAOYSA-N;2,6-Dibromobenzene-1,4-dicarboxylic acid;DB-250889

Suppliers and Price of 2,6-Dibromoterephthalic acid
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
Total 4 raw suppliers
Chemical Property of 2,6-Dibromoterephthalic acid
Chemical Property:
  • PSA:74.60000 
  • LogP:2.60800 
  • XLogP3:2.4
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:2
  • Exact Mass:323.84558
  • Heavy Atom Count:14
  • Complexity:244
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=C(C=C(C(=C1Br)C(=O)O)Br)C(=O)O
Technology Process of 2,6-Dibromoterephthalic acid

There total 1 articles about 2,6-Dibromoterephthalic acid 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 permanganate; In pyridine; water; at 110 ℃; for 12h;
DOI:10.1021/jacs.7b01650
Guidance literature:
With thionyl chloride; N,N-dimethyl-formamide; at 80 ℃; for 3h;
DOI:10.1021/jacs.7b01650
Guidance literature:
Multi-step reaction with 2 steps
1: thionyl chloride; N,N-dimethyl-formamide / 3 h / 80 °C
2: ammonium hydroxide / 1,4-dioxane / 12 h / 20 °C
With ammonium hydroxide; thionyl chloride; N,N-dimethyl-formamide; In 1,4-dioxane;
DOI:10.1021/jacs.7b01650
upstream raw materials:

2,6-dibromo-1,4-dimethylbenzene

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