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5-Bromobenzene-1,2,3-triamine

Base Information
  • Chemical Name:5-Bromobenzene-1,2,3-triamine
  • CAS No.:1121586-23-9
  • Molecular Formula:C6H8BrN3
  • Molecular Weight:202.054
  • Hs Code.:2921590090
  • DSSTox Substance ID:DTXSID40696769
  • Wikidata:Q82626467
  • Mol file:1121586-23-9.mol
5-Bromobenzene-1,2,3-triamine

Synonyms:5-Bromobenzene-1,2,3-triamine;1121586-23-9;5-Bromo-2,3-Diaminoaniline;SCHEMBL12819217;DTXSID40696769;LKRYFTWIURQFJE-UHFFFAOYSA-N;AKOS015995361

Suppliers and Price of 5-Bromobenzene-1,2,3-triamine
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
  • Crysdot
  • 5-Bromobenzene-1,2,3-triamine 95+%
  • 1g
  • $ 455.00
  • American Custom Chemicals Corporation
  • 5-BROMOBENZENE-1,2,3-TRIAMINE 95.00%
  • 5MG
  • $ 503.95
Total 6 raw suppliers
Chemical Property of 5-Bromobenzene-1,2,3-triamine
Chemical Property:
  • Boiling Point:352.7±37.0 °C(Predicted) 
  • PKA:3.79±0.50(Predicted) 
  • PSA:78.06000 
  • Density:1.796±0.06 g/cm3(Predicted) 
  • LogP:2.93930 
  • Storage Temp.:2-8°C 
  • XLogP3:0.6
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:0
  • Exact Mass:200.99016
  • Heavy Atom Count:10
  • Complexity:108
Purity/Quality:

98%min *data from raw suppliers

5-Bromobenzene-1,2,3-triamine 95+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=C(C=C(C(=C1N)N)N)Br
Technology Process of 5-Bromobenzene-1,2,3-triamine

There total 2 articles about 5-Bromobenzene-1,2,3-triamine 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:
4-bromo-2,6-dinitroaniline; With hydrogenchloride; tin(II) chloride dihdyrate; In water; at -20 - 20 ℃;
With water; sodium hydroxide; pH=10;
Guidance literature:
Multi-step reaction with 2 steps
1.1: bromine; acetic acid
2.1: hydrogenchloride; tin(II) chloride dihdyrate / water / -20 - 20 °C
2.2: pH 10
With hydrogenchloride; tin(II) chloride dihdyrate; bromine; acetic acid; In water;
Guidance literature:
Multi-step reaction with 4 steps
1.1: hydrogenchloride / 20 °C / Reflux
1.2: pH 8
2.1: pyridine N-oxide; pyridine; copper diacetate / dichloromethane / 20 - 40 °C / Inert atmosphere
3.1: acetic acid; sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 20 °C
4.1: potassium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1-methyl-pyrrolidin-2-one; water / 0.67 h / 140 °C / Microwave irradiation
With pyridine; pyridine N-oxide; hydrogenchloride; copper diacetate; sodium tris(acetoxy)borohydride; potassium carbonate; acetic acid; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In 1-methyl-pyrrolidin-2-one; dichloromethane; water; 1,2-dichloro-ethane;
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