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Benzylamine, N-(p-chlorobenzylidene)- (6CI,8CI)

Base Information
  • Chemical Name:Benzylamine, N-(p-chlorobenzylidene)- (6CI,8CI)
  • CAS No.:13540-93-7
  • Molecular Formula:C14H12ClN
  • Molecular Weight:229.709
  • Hs Code.:
  • Mol file:13540-93-7.mol
Benzylamine, N-(p-chlorobenzylidene)- (6CI,8CI)

Synonyms:Benzylamine,N-(p-chlorobenzylidene);N-(p-chlorobenzylidene)benzylamine;Benzenemethanamine,N-[(4-chlorophenyl)methylene];p-chlorobenzylidene-benzyl-amine;N-(benzylidene)-p-chlorobenzylamine;p-chlorobenzylidene benzylimine;4-chlorobenzaldehyde-N-benzylimine;N-(4-chlorobenzylidene)-1-phenylmethanamine;N-benzyl-(4-chlorophenyl)methanimine;N-(4-chlorobenzylidene)benzylamine;

Suppliers and Price of Benzylamine, N-(p-chlorobenzylidene)- (6CI,8CI)
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 3 raw suppliers
Chemical Property of Benzylamine, N-(p-chlorobenzylidene)- (6CI,8CI)
Chemical Property:
  • Melting Point:34-36℃ 
  • PSA:12.36000 
  • LogP:3.95910 
Purity/Quality:

98% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of Benzylamine, N-(p-chlorobenzylidene)- (6CI,8CI)

There total 21 articles about Benzylamine, N-(p-chlorobenzylidene)- (6CI,8CI) 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:
for 6h; Molecular sieve; Reflux;
DOI:10.1021/jacs.9b09395
Guidance literature:
With oxygen; sodium hydroxide; In tetrahydrofuran; 2,2,2-trifluoroethanol; at 30 ℃; for 12h;
DOI:10.1039/c2cc36213a
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