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4-Nitrobenzohydroxamic acid

Base Information Edit
  • Chemical Name:4-Nitrobenzohydroxamic acid
  • CAS No.:1613-76-9
  • Molecular Formula:C7H6 N2 O4
  • Molecular Weight:182.136
  • Hs Code.:2924299090
  • UNII:R73HGY95CM
  • ChEMBL ID:CHEMBL155132
  • DSSTox Substance ID:DTXSID20167109
  • NSC Number:682753,13998
  • Wikidata:Q83036427
  • Mol file:1613-76-9.mol
4-Nitrobenzohydroxamic acid

Synonyms:4-nitrobenzohydroxamic acid

Suppliers and Price of 4-Nitrobenzohydroxamic acid
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 4 raw suppliers
Chemical Property of 4-Nitrobenzohydroxamic acid Edit
Chemical Property:
  • Melting Point:130oC 
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:95.15000 
  • Density:1.485g/cm3 
  • LogP:1.62790 
  • XLogP3:0.6
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:1
  • Exact Mass:182.03275668
  • Heavy Atom Count:13
  • Complexity:205
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=CC=C1C(=O)NO)[N+](=O)[O-]
Technology Process of 4-Nitrobenzohydroxamic acid

There total 16 articles about 4-Nitrobenzohydroxamic 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 Nafion-H; In isopropyl alcohol; for 20h; Heating;
DOI:10.1021/jo0256890
Guidance literature:
With N-Bromosuccinimide; hydroxylamine hydrochloride; triphenylphosphine; In triethylamine; acetonitrile; at 20 ℃; for 2h;
DOI:10.1002/jccs.200000140

Reference yield: 90.0%

Guidance literature:
With potassium hydroxide; hydroxylamine; In methanol; at 20 ℃; for 12h; pH=10;
DOI:10.1039/b822806j
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