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N-(2-naphthyl)benzimidoyl chloride

Base Information
  • Chemical Name:N-(2-naphthyl)benzimidoyl chloride
  • CAS No.:1934-88-9
  • Molecular Formula:C17H12ClN
  • Molecular Weight:265.742
  • Hs Code.:
  • DSSTox Substance ID:DTXSID201253648
  • Mol file:1934-88-9.mol
N-(2-naphthyl)benzimidoyl chloride

Synonyms:N-(2-naphthyl)benzimidoyl chloride;DTXSID201253648;1934-88-9;N-2-Naphthalenylbenzenecarboximidoyl chloride

Suppliers and Price of N-(2-naphthyl)benzimidoyl chloride
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 1 raw suppliers
Chemical Property of N-(2-naphthyl)benzimidoyl chloride
Chemical Property:
  • XLogP3:5.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:2
  • Exact Mass:265.0658271
  • Heavy Atom Count:19
  • Complexity:319
Purity/Quality:

95% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C(=NC2=CC3=CC=CC=C3C=C2)Cl
Technology Process of N-(2-naphthyl)benzimidoyl chloride

There total 2 articles about N-(2-naphthyl)benzimidoyl chloride 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:
With phosphorus pentachloride;
Guidance literature:
2-Benzamino-naphthalin, Phosphor(V)-chlorid, Δ;
Guidance literature:
5-Phenyl-1H-tetrazole; N-(2-naphthyl)benzimidoyl chloride; With sodium hydroxide; tetrabutylammomium bromide; In chloroform; at 20 ℃; for 4h;
In toluene; at 110 ℃; for 2h;
DOI:10.1007/s11178-005-0087-0
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