N-(4-Methylphenyl)benzenecarboximidoyl chloride

Base Information

Chemical Name:N-(4-Methylphenyl)benzenecarboximidoyl chloride
CAS No.:15999-95-8
Molecular Formula:C14H12ClN
Molecular Weight:229.709
Hs Code.:
DSSTox Substance ID:DTXSID80575867
Nikkaji Number:J1.150.566J
Mol file:15999-95-8.mol

Synonyms:N-(4-Methylphenyl)benzenecarboximidoyl chloride;15999-95-8;N-p-tolylbenzimidoyl chlo-ride;DTXSID80575867;N-(4-methylphenyl)benzimidoyl chloride

Suppliers and Price of N-(4-Methylphenyl)benzenecarboximidoyl 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-(4-Methylphenyl)benzenecarboximidoyl chloride

Chemical Property:

XLogP3:4.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:229.0658271
Heavy Atom Count:16
Complexity:235

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)N=C(C2=CC=CC=C2)Cl

Technology Process of N-(4-Methylphenyl)benzenecarboximidoyl chloride

There total 6 articles about N-(4-Methylphenyl)benzenecarboximidoyl 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:

Reference yield: 98.0%

: 582-78-5
N-(4-methylphenyl)benzamide

: 15999-95-8
4-methylphenylbenzimidoyl chloride

Guidance literature:: With thionyl chloride; for 4h; Heating;

Reference yield:

: 106-49-0,12221-03-3
p-toluidine

: 15999-95-8
4-methylphenylbenzimidoyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 48 h / Reflux

2: thionyl chloride / 3 h / Reflux

With thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1039/c1nj20343f

Reference yield:

: 98-88-4
benzoyl chloride

: 15999-95-8
4-methylphenylbenzimidoyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 48 h / Reflux

2: thionyl chloride / 3 h / Reflux

With thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1039/c1nj20343f