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1,5-Diaminobromo-4,8-dihydroxyanthraquinone

Base Information Edit
  • Chemical Name:1,5-Diaminobromo-4,8-dihydroxyanthraquinone
  • CAS No.:27312-17-0
  • Deprecated CAS:234443-10-8,37099-98-2,53127-11-0,54847-48-2,55070-31-0,60327-79-9,73468-51-6,95032-03-4,120920-38-9,375793-87-6
  • Molecular Formula:C14H9 Br N2 O4
  • Molecular Weight:349.14
  • Hs Code.:
  • European Community (EC) Number:248-395-0,250-817-3
  • UNII:K26YA0E1FU
  • DSSTox Substance ID:DTXSID9067300
  • Nikkaji Number:J55.271B
  • Wikidata:Q81993878
  • Mol file:27312-17-0.mol
1,5-Diaminobromo-4,8-dihydroxyanthraquinone

Synonyms:Disperse blue polyether

Suppliers and Price of 1,5-Diaminobromo-4,8-dihydroxyanthraquinone
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 5 raw suppliers
Chemical Property of 1,5-Diaminobromo-4,8-dihydroxyanthraquinone Edit
Chemical Property:
  • Vapor Pressure:4.62E-19mmHg at 25°C 
  • Refractive Index:1.6100 (estimate) 
  • Boiling Point:679.1°C at 760 mmHg 
  • PKA:5.68±0.20(Predicted) 
  • Flash Point:364.5°C 
  • PSA:126.64000 
  • Density:1.976g/cm3 
  • LogP:2.96250 
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:0
  • Exact Mass:347.97457
  • Heavy Atom Count:21
  • Complexity:474
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=C2C(=C1N)C(=O)C3=C(C2=O)C(=C(C=C3O)Br)N)O
  • Uses 1,5-Diamino-2-bromo-4,8-dihydroxy-9,10-anthracenedione is an anthraquinone disperse dyes.
Technology Process of 1,5-Diaminobromo-4,8-dihydroxyanthraquinone

There total 1 articles about 1,5-Diaminobromo-4,8-dihydroxyanthraquinone 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:
Anthrachinon I, Br2;
Guidance literature:
With potassium hydroxide; In water; N,N-dimethyl-formamide; at 120 - 125 ℃; for 3h;
Guidance literature:
With potassium hydroxide; In water; N,N-dimethyl-formamide; at 120 - 125 ℃; for 3h;
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