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5-Amino-3-bromo-2-nitrobenzoic acid

Base Information
  • Chemical Name:5-Amino-3-bromo-2-nitrobenzoic acid
  • CAS No.:60912-51-8
  • Molecular Formula:C7H5BrN2O4
  • Molecular Weight:261.03
  • Hs Code.:2922499990
  • DSSTox Substance ID:DTXSID60415419
  • Wikidata:Q82224343
  • Mol file:60912-51-8.mol
5-Amino-3-bromo-2-nitrobenzoic acid

Synonyms:5-amino-3-bromo-2-nitrobenzoic acid;60912-51-8;Benzoic acid,5-amino-3-bromo-2-nitro-;DTXSID60415419;FT-0709133

Suppliers and Price of 5-Amino-3-bromo-2-nitrobenzoic 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
  • American Custom Chemicals Corporation
  • 5-AMINO-3-BROMO-2-NITRO-BENZOICACID 95.00%
  • 5MG
  • $ 504.04
Total 9 raw suppliers
Chemical Property of 5-Amino-3-bromo-2-nitrobenzoic acid
Chemical Property:
  • Vapor Pressure:1.45E-09mmHg at 25°C 
  • Refractive Index:1.709 
  • Boiling Point:468.1 °C at 760 mmHg 
  • Flash Point:236.9 °C 
  • PSA:109.14000 
  • Density:1.973 g/cm3 
  • LogP:2.74210 
  • XLogP3:1.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:1
  • Exact Mass:259.94327
  • Heavy Atom Count:14
  • Complexity:255
Purity/Quality:

98%Min *data from raw suppliers

5-AMINO-3-BROMO-2-NITRO-BENZOICACID 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=C(C=C(C(=C1C(=O)O)[N+](=O)[O-])Br)N
Technology Process of 5-Amino-3-bromo-2-nitrobenzoic acid

There total 5 articles about 5-Amino-3-bromo-2-nitrobenzoic 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 water; barium(II) hydroxide; In methanol; for 18h; Reflux;
DOI:10.1016/j.mencom.2020.11.006
Guidance literature:
Multi-step reaction with 4 steps
1: thionyl chloride / 2 h / 0 - 25 °C / Reflux
2: triethylamine; dmap / tetrahydrofuran / 25 °C
3: nitric acid; sulfuric acid / 0.5 h / 0 - 25 °C
4: barium(II) hydroxide; water / methanol / 18 h / Reflux
With dmap; thionyl chloride; sulfuric acid; water; nitric acid; triethylamine; barium(II) hydroxide; In tetrahydrofuran; methanol;
DOI:10.1016/j.mencom.2020.11.006
Guidance literature:
Multi-step reaction with 3 steps
1: triethylamine; dmap / tetrahydrofuran / 25 °C
2: nitric acid; sulfuric acid / 0.5 h / 0 - 25 °C
3: barium(II) hydroxide; water / methanol / 18 h / Reflux
With dmap; sulfuric acid; water; nitric acid; triethylamine; barium(II) hydroxide; In tetrahydrofuran; methanol;
DOI:10.1016/j.mencom.2020.11.006
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