1H-Imidazole-2-carboxamide, 1-methyl-N-phenyl-

Base Information

Chemical Name:1H-Imidazole-2-carboxamide, 1-methyl-N-phenyl-
CAS No.:35342-94-0
Molecular Formula:C11H11N3O
Molecular Weight:201.228
Hs Code.:
DSSTox Substance ID:DTXSID10392428
Nikkaji Number:J1.483.196G
Wikidata:Q82190652

Synonyms:35342-94-0;1h-imidazole-2-carboxamide,1-methyl-n-phenyl-;1H-Imidazole-2-carboxamide, 1-methyl-N-phenyl-;SCHEMBL14583507;DTXSID10392428;N-Phenyl-1-methyl-1H-imidazole-2-carboxamide

Suppliers and Price of 1H-Imidazole-2-carboxamide, 1-methyl-N-phenyl-

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 0 raw suppliers

Chemical Property of 1H-Imidazole-2-carboxamide, 1-methyl-N-phenyl-

Chemical Property:

XLogP3:1.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:201.090211983
Heavy Atom Count:15
Complexity:226

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1C=CN=C1C(=O)NC2=CC=CC=C2

Technology Process of 1H-Imidazole-2-carboxamide, 1-methyl-N-phenyl-

There total 5 articles about 1H-Imidazole-2-carboxamide, 1-methyl-N-phenyl- 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: 24.0%

: 616-47-7
1-methyl-1H-imidazole

: 103-71-9
phenyl isocyanate

: 35342-94-0
1-methyl-N-phenyl-1H-imidazole-2-carboxamide

: 103-70-8
Formanilid

Guidance literature:: With dodecacarbonyltetrairidium; diethylmethylsilane; In toluene; at 110 ℃; for 6h; regioselective reaction;
DOI:10.1055/a-1375-5283

Reference yield:

: 20062-51-5
1-methyl-1H-imidazole-2-carboxamide

: 2996-92-1,46143-12-8
phenyl trimethylsiloxane

: 35342-94-0
1-methyl-N-phenyl-1H-imidazole-2-carboxamide

: 1-methyl-1H-imidazole-2-carboxylic acid diphenylamide

Guidance literature:: With tetrabutyl ammonium fluoride; copper diacetate; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1016/S0040-4039(01)00203-9

Reference yield:

: 103-71-9
phenyl isocyanate

: 35342-94-0
1-methyl-N-phenyl-1H-imidazole-2-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: CHCl₃ / 24 h / 65 °C

2: aq. HCl

3: 55 percent / aq. HCl; NaNO₂ / 0.5 h / 0 °C / cooling

With hydrogenchloride; sodium nitrite; In chloroform;
DOI:10.3987/COM-06-10836