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Technology Process of 2,6-dichloro-N-[(2,4-dichlorophenyl)carbamoyl]-4-methylpyridine-3-carboxamide

2,6-dichloro-N-[(2,4-dichlorophenyl)carbamoyl]-4-methylpyridine-3-carboxamide

Base Information
  • Chemical Name:2,6-dichloro-N-[(2,4-dichlorophenyl)carbamoyl]-4-methylpyridine-3-carboxamide
  • CAS No.:286430-78-2
  • Molecular Formula:C14H9 Cl4 N3 O2
  • Molecular Weight:393.05
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10381852
  • Wikidata:Q82172976
  • Mol file:286430-78-2.mol
2,6-dichloro-N-[(2,4-dichlorophenyl)carbamoyl]-4-methylpyridine-3-carboxamide

Synonyms:286430-78-2;2,6-dichloro-N-[(2,4-dichlorophenyl)carbamoyl]-4-methylpyridine-3-carboxamide;N-[(2,6-dichloro-4-methyl-3-pyridyl)carbonyl]-N'-(2,4-dichlorophenyl)urea;3-Pyridinecarboxamide, 2,6-dichloro-N-[[(2,4-dichlorophenyl)amino]carbonyl]-4-methyl-;DTXSID10381852;FT-0749204;2,6-Dichloro-N-[(2,4-dichlorophenyl)carbamoyl]-4-methylnicotinamide

Suppliers and Price of 2,6-dichloro-N-[(2,4-dichlorophenyl)carbamoyl]-4-methylpyridine-3-carboxamide
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
  • American Custom Chemicals Corporation
  • N-[(2,6-DICHLORO-4-METHYL-3-PYRIDYL)CARBONYL]-N'-(2,4-DICHLOROPHENYL)UREA 95.00%
  • 5MG
  • $ 501.30
Total 2 raw suppliers
Chemical Property of 2,6-dichloro-N-[(2,4-dichlorophenyl)carbamoyl]-4-methylpyridine-3-carboxamide
Chemical Property:
  • PSA：78.07000 
  • LogP:5.55390 
  • XLogP3:5.4
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:392.941937
  • Heavy Atom Count:23
  • Complexity:454
Purity/Quality:

95% *data from raw suppliers

N-[(2,6-DICHLORO-4-METHYL-3-PYRIDYL)CARBONYL]-N'-(2,4-DICHLOROPHENYL)UREA 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC(=NC(=C1C(=O)NC(=O)NC2=C(C=C(C=C2)Cl)Cl)Cl)Cl
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