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Technology Process of 2-Methoxy-4-[(4-nitrophenyl)azo]aniline

2-Methoxy-4-[(4-nitrophenyl)azo]aniline

Base Information
  • Chemical Name:2-Methoxy-4-[(4-nitrophenyl)azo]aniline
  • CAS No.:101-52-0
  • Molecular Formula:C13H12 N4 O3
  • Molecular Weight:272.25938
  • Hs Code.:
  • European Community (EC) Number:202-949-8
  • UNII:75MKE5QS7Q
  • DSSTox Substance ID:DTXSID6059233
  • Nikkaji Number:J30.283J
  • Mol file:101-52-0.mol
2-Methoxy-4-[(4-nitrophenyl)azo]aniline

Synonyms:101-52-0;2-Methoxy-4-[(4-nitrophenyl)azo]aniline;4-((4-Nitrophenyl)azo)-o-anisidine;2-methoxy-4-[(4-nitrophenyl)diazenyl]aniline;75MKE5QS7Q;4-Amino-3-methoxy-4'-nitroazobenzene;2-Methoxy-4-((4-nitrophenyl)azo)aniline;4-[(4-NITROPHENYL)AZO]-O-ANISIDINE;Benzenamine, 2-methoxy-4-(2-(4-nitrophenyl)diazenyl)-;Benzenamine, 2-methoxy-4-[2-(4-nitrophenyl)diazenyl]-;2-METHOXY-4-((4-NITROPHENYL)DIAZENYL)ANILINE;EINECS 202-949-8;UNII-75MKE5QS7Q;DTXSID6059233;SCHEMBL11577927;SCHEMBL14704228;4-((P-NITROPHENYL)AZO)-O-ANISIDINE;O-ANISIDINE, 4-((P-NITROPHENYL)AZO)-;Benzenamine, 2-methoxy-4-((4-nitrophenyl)azo)-;2-METHOXY-4-(2-(4-NITROPHENYL)DIAZENYL)BENZENAMINE

Suppliers and Price of 2-Methoxy-4-[(4-nitrophenyl)azo]aniline
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
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Total 10 raw suppliers
Chemical Property of 2-Methoxy-4-[(4-nitrophenyl)azo]aniline
Chemical Property:
  • Vapor Pressure:7.69E-10mmHg at 25°C 
  • Melting Point:243 °C 
  • Boiling Point:492.4°C at 760 mmHg 
  • PKA:2.73±0.10(Predicted) 
  • Flash Point:251.6°C 
  • Density:1.34g/cm3 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:3
  • Exact Mass:272.09094026
  • Heavy Atom Count:20
  • Complexity:350
Purity/Quality:

98%,99%, *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:COC1=C(C=CC(=C1)N=NC2=CC=C(C=C2)[N+](=O)[O-])N
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