N(sup 1)-(4-Chlorophenyl)-N(sup 2)-phenyl-1H-imidazole-1,2-dicarboxamide

Base Information

Chemical Name:N(sup 1)-(4-Chlorophenyl)-N(sup 2)-phenyl-1H-imidazole-1,2-dicarboxamide
CAS No.:139109-17-4
Molecular Formula:C17H13ClN4O2
Molecular Weight:340.7637
Hs Code.:
DSSTox Substance ID:DTXSID80160914
Wikidata:Q83029253

Synonyms:N(sup 1)-(4-Chlorophenyl)-N(sup 2)-phenyl-1H-imidazole-1,2-dicarboxamide;1H-Imidazole-1,2-dicarboxamide, N(sup 1)-(4-chlorophenyl)-N(sup 2)-phenyl-;1-(N-p-Chlorophenyl)-2-(N-phenyl)imidazole-1,2-dicarboxamide;139109-17-4;DTXSID80160914;LS-78352

Suppliers and Price of N(sup 1)-(4-Chlorophenyl)-N(sup 2)-phenyl-1H-imidazole-1,2-dicarboxamide

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
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Total 0 raw suppliers

Chemical Property of N(sup 1)-(4-Chlorophenyl)-N(sup 2)-phenyl-1H-imidazole-1,2-dicarboxamide

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.36g/cm³
XLogP3:3.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:340.0727034
Heavy Atom Count:24
Complexity:448

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)NC(=O)C2=NC=CN2C(=O)NC3=CC=C(C=C3)Cl

Technology Process of N(sup 1)-(4-Chlorophenyl)-N(sup 2)-phenyl-1H-imidazole-1,2-dicarboxamide

There total 2 articles about N(sup 1)-(4-Chlorophenyl)-N(sup 2)-phenyl-1H-imidazole-1,2-dicarboxamide 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:

: 104-12-1
p-chlorphenylisocyanate

: 139109-17-4
1-(N-p-chlorophenyl)-2-(N-phenyl)imidazole-1,2-dicarboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: CHCl₃ / Ambient temperature

2: nitrobenzene / 5 h / Heating

In chloroform; nitrobenzene;