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Acetamide, N-(3-amino-2-hydroxy-5-nitrophenyl)-

Base Information
  • Chemical Name:Acetamide, N-(3-amino-2-hydroxy-5-nitrophenyl)-
  • CAS No.:6358-63-0
  • Molecular Formula:C8H9 N3 O4
  • Molecular Weight:211.177
  • Hs Code.:2924299090
  • European Community (EC) Number:228-781-5
  • UNII:HH2SGW7W9G
  • DSSTox Substance ID:DTXSID0064252
  • Nikkaji Number:J60.155A
  • Wikidata:Q81991375
  • Mol file:6358-63-0.mol
Acetamide, N-(3-amino-2-hydroxy-5-nitrophenyl)-

Synonyms:N-(3-Amino-2-hydroxy-5-nitrophenyl)acetamide;6358-63-0;Acetamide, N-(3-amino-2-hydroxy-5-nitrophenyl)-;EINECS 228-781-5;Acetanilide, 3'-amino-2'-hydroxy-5'-nitro-;HH2SGW7W9G;SCHEMBL2791838;DTXSID0064252;SCHEMBL13997712;2-Acetamido-6-amino-4-nitrophenol;6-Acetylamino-2-amino-4-nitrophenol

Suppliers and Price of Acetamide, N-(3-amino-2-hydroxy-5-nitrophenyl)-
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 20 raw suppliers
Chemical Property of Acetamide, N-(3-amino-2-hydroxy-5-nitrophenyl)-
Chemical Property:
  • Vapor Pressure:7.43E-10mmHg at 25°C 
  • Boiling Point:480.5°C at 760 mmHg 
  • Flash Point:244.4°C 
  • PSA:121.17000 
  • Density:1.563g/cm3 
  • LogP:2.01840 
  • XLogP3:-0.1
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:1
  • Exact Mass:211.05930578
  • Heavy Atom Count:15
  • Complexity:265
Purity/Quality:

99% ,98%,Electron Grade , *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=O)NC1=CC(=CC(=C1O)N)[N+](=O)[O-]
Technology Process of Acetamide, N-(3-amino-2-hydroxy-5-nitrophenyl)-

There total 2 articles about Acetamide, N-(3-amino-2-hydroxy-5-nitrophenyl)- 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:
Multi-step reaction with 2 steps
1: natrium carbonate / 60 °C
2: sulfuralkali
With sulfuralkali; sodium carbonate;
upstream raw materials:

acetic acid-(2-hydroxy-3,5-dinitro-anilide)

picramic acid

Downstream raw materials:

2,6-diamino-4-nitrophenol

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