1H-Benzimidazole-5-carboxamide, N-(phenylmethyl)-

Base Information

Chemical Name:1H-Benzimidazole-5-carboxamide, N-(phenylmethyl)-
CAS No.:142535-86-2
Molecular Formula:C15H13N3O
Molecular Weight:
Hs Code.:
DSSTox Substance ID:DTXSID80438620
Wikidata:Q82254416

Synonyms:1H-Benzimidazole-5-carboxamide, N-(phenylmethyl)-;142535-86-2;SCHEMBL3153245;DTXSID80438620;WUYMGCRGXHBGBY-UHFFFAOYSA-N;AKOS002854335;N-Benzyl-1H-benzimidazole-5-carboxamide;1H-benzimidazole-5-carboxylic acid benzylamide;Z27749674

Suppliers and Price of 1H-Benzimidazole-5-carboxamide, N-(phenylmethyl)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 1H-Benzimidazole-5-carboxamide, N-(phenylmethyl)-

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:251.105862047
Heavy Atom Count:19
Complexity:315

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CNC(=O)C2=CC3=C(C=C2)N=CN3

Technology Process of 1H-Benzimidazole-5-carboxamide, N-(phenylmethyl)-

There total 1 articles about 1H-Benzimidazole-5-carboxamide, 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: 66.0%

: 142535-86-2
5-(benzylaminocarboxy)benzimidazole

Guidance literature:

Reference yield:

: 142535-86-2
5-(benzylaminocarboxy)benzimidazole

: 127166-64-7
11-[2-(6-Benzylcarbamoyl-benzoimidazol-1-yl)-eth-(E)-ylidene]-6,11-dihydro-dibenzo[b,e]oxepine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: toluene; dimethylformamide / 3 h / Heating

2: NaOH / methanol; H₂O / 1.5 h / Heating

With sodium hydroxide; In methanol; water; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jm00096a017

Reference yield:

: 142535-86-2
5-(benzylaminocarboxy)benzimidazole

: 127166-63-6
(E)-11-[2-[5-(N-benzylcarbamoyl)-1-benzimidazolyl]ethylidene]-6,11-dihydrodibenz[b,e]oxepin-2-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: toluene; dimethylformamide / 3 h / Heating

2: NaOH / methanol; H₂O / 1.5 h / Heating

With sodium hydroxide; In methanol; water; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jm00096a017