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Technology Process of 2-(N-(2-Cyanoethyl)-4-((2,6-dichloro-4-nitrophenyl)azo)-3-methylanilino)ethyl acetate

2-(N-(2-Cyanoethyl)-4-((2,6-dichloro-4-nitrophenyl)azo)-3-methylanilino)ethyl acetate

Base Information
  • Chemical Name:2-(N-(2-Cyanoethyl)-4-((2,6-dichloro-4-nitrophenyl)azo)-3-methylanilino)ethyl acetate
  • CAS No.:79154-84-0
  • Molecular Formula:C20H19 Cl2 N5 O4
  • Molecular Weight:464.30196
  • Hs Code.:
  • European Community (EC) Number:279-101-9
  • DSSTox Substance ID:DTXSID301112607
  • Nikkaji Number:J319.240G
  • Mol file:79154-84-0.mol
2-(N-(2-Cyanoethyl)-4-((2,6-dichloro-4-nitrophenyl)azo)-3-methylanilino)ethyl acetate

Synonyms:79154-84-0;EINECS 279-101-9;2-(N-(2-Cyanoethyl)-4-((2,6-dichloro-4-nitrophenyl)azo)-3-methylanilino)ethyl acetate;2-[N-(2-Cyanoethyl)-4-[(2,6-dichloro-4-nitrophenyl)azo]-3-methylanilino]ethyl acetate;DTXSID301112607;3-[(2-Acetoxyethyl)[4-[(2,6-dichloro-4-nitrophenyl)azo]-3-methylphenyl]amino]propanenitrile;3-[[2-(Acetyloxy)ethyl][4-[2-(2,6-dichloro-4-nitrophenyl)diazenyl]-3-methylphenyl]amino]propanenitrile

Suppliers and Price of 2-(N-(2-Cyanoethyl)-4-((2,6-dichloro-4-nitrophenyl)azo)-3-methylanilino)ethyl acetate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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  • Chemicals and raw materials
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Total 3 raw suppliers
Chemical Property of 2-(N-(2-Cyanoethyl)-4-((2,6-dichloro-4-nitrophenyl)azo)-3-methylanilino)ethyl acetate
Chemical Property:
  • Vapor Pressure:5.29E-17mmHg at 25°C 
  • Boiling Point:654.4°C at 760 mmHg 
  • Flash Point:349.6°C 
  • PSA：123.87000 
  • Density:1.36g/cm3 
  • LogP:6.43178 
  • XLogP3:4.8
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:9
  • Exact Mass:463.0814095
  • Heavy Atom Count:31
  • Complexity:683
Purity/Quality:

85.0-99.8% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=C(C=CC(=C1)N(CCC#N)CCOC(=O)C)N=NC2=C(C=C(C=C2Cl)[N+](=O)[O-])Cl
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