Benzenecarboximidoyl chloride, 4-nitro-N-(phenylmethyl)-

Base Information

Chemical Name:Benzenecarboximidoyl chloride, 4-nitro-N-(phenylmethyl)-
CAS No.:3712-57-0
Molecular Formula:C14H11ClN2O2
Molecular Weight:274.707
Hs Code.:
DSSTox Substance ID:DTXSID20455533
Nikkaji Number:J917.290D
Mol file:3712-57-0.mol

Synonyms:3712-57-0;Benzenecarboximidoyl chloride, 4-nitro-N-(phenylmethyl)-;DTXSID20455533;N-Benzyl-4-nitrobenzimidic acid chloride

Suppliers and Price of Benzenecarboximidoyl chloride, 4-nitro-N-(phenylmethyl)-

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 Benzenecarboximidoyl chloride, 4-nitro-N-(phenylmethyl)-

Chemical Property:

XLogP3:4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:274.0509053
Heavy Atom Count:19
Complexity:327

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CN=C(C2=CC=C(C=C2)[N+](=O)[O-])Cl

Technology Process of Benzenecarboximidoyl chloride, 4-nitro-N-(phenylmethyl)-

There total 7 articles about Benzenecarboximidoyl chloride, 4-nitro-N-(phenylmethyl)- 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:

: 2585-26-4
4-nitro-N-benzylbenzamide

: 3712-57-0
N-benzyl-4-nitrobenzimidoyl chloride

Guidance literature:: With thionyl chloride; for 2h; Reflux;
DOI:10.1016/j.ejmech.2014.02.041

Reference yield:

: 122-04-3
4-nitro-benzoyl chloride

: 3712-57-0
N-(benzyl)-4-nitrobenzimidoyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / pyridine / 1 h / 90 °C

2: SOCl₂ / Heating

With thionyl chloride; In pyridine;
DOI:10.1002/1522-2675(200204)85:4<1102::AID-HLCA1102>3.0.CO;2-T

Reference yield:

: 100-46-9
benzylamine

: 3712-57-0
N-(benzyl)-4-nitrobenzimidoyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / pyridine / 1 h / 90 °C

2: SOCl₂ / Heating

With thionyl chloride; In pyridine;
DOI:10.1002/1522-2675(200204)85:4<1102::AID-HLCA1102>3.0.CO;2-T