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Technology Process of 2-Naphthalenecarboxamide, 4-[(4-chloro-2-methylphenyl)azo]-N-(2-ethylphenyl)-3-hydroxy-

2-Naphthalenecarboxamide, 4-[(4-chloro-2-methylphenyl)azo]-N-(2-ethylphenyl)-3-hydroxy-

Base Information
  • Chemical Name:2-Naphthalenecarboxamide, 4-[(4-chloro-2-methylphenyl)azo]-N-(2-ethylphenyl)-3-hydroxy-
  • CAS No.:74186-12-2
  • Molecular Formula:C26H22 Cl N3 O2
  • Molecular Weight:443.92478
  • Hs Code.:
  • European Community (EC) Number:277-750-2
  • DSSTox Substance ID:DTXSID9072785
  • Nikkaji Number:J318.924D
  • Mol file:74186-12-2.mol
2-Naphthalenecarboxamide, 4-[(4-chloro-2-methylphenyl)azo]-N-(2-ethylphenyl)-3-hydroxy-

Synonyms:74186-12-2;EINECS 277-750-2;2-Naphthalenecarboxamide, 4-[(4-chloro-2-methylphenyl)azo]-N-(2-ethylphenyl)-3-hydroxy-;1-((2-Methyl-4-chlorophenyl)azo)-2-hydroxy-3-naphthoic acid, o-ethylanilide;2-Naphthalenecarboxamide, 4-((4-chloro-2-methylphenyl)azo)-N-(2-ethylphenyl)-3-hydroxy-;2-Naphthalenecarboxamide, 4-(2-(4-chloro-2-methylphenyl)diazenyl)-N-(2-ethylphenyl)-3-hydroxy-;4-((4-Chloro-2-methylphenyl)azo)-N-(2-ethylphenyl)-3-hydroxynaphthalene-2-carboxamide;4-[(4-CHLORO-2-METHYLPHENYL)AZO]-N-(2-ETHYLPHENYL)-3-HYDROXYNAPHTHALENE-2-CARBOXAMIDE;DTXSID9072785;4-[(4-Chloro-2-methylphenyl)azo]-N-(2-ethylphenyl)-3-hydroxy-2-naphthalenecarboxamide

Suppliers and Price of 2-Naphthalenecarboxamide, 4-[(4-chloro-2-methylphenyl)azo]-N-(2-ethylphenyl)-3-hydroxy-
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 3 raw suppliers
Chemical Property of 2-Naphthalenecarboxamide, 4-[(4-chloro-2-methylphenyl)azo]-N-(2-ethylphenyl)-3-hydroxy-
Chemical Property:
  • Density:1.258g/cm3 
  • XLogP3:7.8
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:5
  • Exact Mass:443.1400546
  • Heavy Atom Count:32
  • Complexity:659
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCC1=CC=CC=C1NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=C(C=C(C=C4)Cl)C
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