2-(3-Aminophenyl)-1H-benzimidazole-5-carboxylic acid

Base Information

Chemical Name:2-(3-Aminophenyl)-1H-benzimidazole-5-carboxylic acid
CAS No.:190121-98-3
Molecular Formula:C14H11 N3 O2
Molecular Weight:0
Hs Code.:
DSSTox Substance ID:DTXSID00356933
Wikidata:Q82136575
Mol file:190121-98-3.mol

Synonyms:190121-98-3;2-(3-AMINOPHENYL)-1H-BENZIMIDAZOLE-5-CARBOXYLIC ACID;2-(3-aminophenyl)-3H-benzimidazole-5-carboxylic acid;2-(3-Aminophenyl)-1H-benzo[d]imidazole-6-carboxylic acid;Oprea1_120284;Oprea1_823705;DTXSID00356933;2-(3-Aminophenyl)-1H-benzimidazole-6-carboxylic acid;1H-Benzimidazole-6-carboxylic acid, 2-(3-aminophenyl)-;2-(3-aminophenyl)-1h-benzo[d]imidazole-5-carboxylic acid

Suppliers and Price of 2-(3-Aminophenyl)-1H-benzimidazole-5-carboxylic acid

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 1 raw suppliers

Chemical Property of 2-(3-Aminophenyl)-1H-benzimidazole-5-carboxylic acid

Chemical Property:

PSA：92.00000
LogP:3.09150
XLogP3:2.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:253.085126602
Heavy Atom Count:19
Complexity:350

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC(=C1)N)C2=NC3=C(N2)C=C(C=C3)C(=O)O

Technology Process of 2-(3-Aminophenyl)-1H-benzimidazole-5-carboxylic acid

There total 3 articles about 2-(3-Aminophenyl)-1H-benzimidazole-5-carboxylic acid 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: 54.9%

: 180197-42-6
1H-2-(3-nitrophenyl)benzimidazole-5-carboxylic acid

: 190121-98-3
2-(3-aminophenyl)benzimidazole-5-carboxylic acid

Guidance literature:: With hydrogenchloride; hydrogen; palladium on activated charcoal; In methanol; under 3000.2 Torr;

Reference yield:

: 99-61-6
3-nitro-benzaldehyde

: 190121-98-3
2-(3-aminophenyl)benzimidazole-5-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 2) O₂ / 1) EtOH, reflux, 1 h, 2) EtOH, 150 deg C, 6 bar, 24 h

2: 54.9 percent / H₂, 2 N HCl / Pd/C / methanol / 3000.2 Torr

With hydrogenchloride; hydrogen; oxygen; palladium on activated charcoal; In methanol;

Reference yield:

: 619-05-6
3,4-diaminobenzoic acid

: 190121-98-3
2-(3-aminophenyl)benzimidazole-5-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 2) O₂ / 1) EtOH, reflux, 1 h, 2) EtOH, 150 deg C, 6 bar, 24 h

2: 54.9 percent / H₂, 2 N HCl / Pd/C / methanol / 3000.2 Torr

With hydrogenchloride; hydrogen; oxygen; palladium on activated charcoal; In methanol;