4-Amino-N-1H-benzimidazol-2-yl-benzenesulfonamide

Base Information

Chemical Name:4-Amino-N-1H-benzimidazol-2-yl-benzenesulfonamide
CAS No.:52715-11-4
Molecular Formula:C13H12 N4 O2 S
Molecular Weight:288.325
Hs Code.:
DSSTox Substance ID:DTXSID20200686
Nikkaji Number:J861.509H
Wikidata:Q83073835
ChEMBL ID:CHEMBL11886

Synonyms:52715-11-4;4-Amino-N-1H-benzimidazol-2-yl-benzenesulfonamide;4-Amino-N-(1H-benzo[d]imidazol-2-yl)benzenesulfonamide;4-amino-N-(1H-benzimidazol-2-yl)benzenesulfonamide;CHEMBL11886;DTXSID20200686;AKOS012872144;N-[1H-Benzimidazol-2(3H)-ylidene]-4-aminobenzenesulfonamide

Suppliers and Price of 4-Amino-N-1H-benzimidazol-2-yl-benzenesulfonamide

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 4-Amino-N-1H-benzimidazol-2-yl-benzenesulfonamide

Chemical Property:

Vapor Pressure:2.25E-13mmHg at 25°C
Boiling Point:578.4°Cat760mmHg
Flash Point:303.6°C
Density:1.546g/cm³
XLogP3:1.7
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:288.06809681
Heavy Atom Count:20
Complexity:428

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)NC(=N2)NS(=O)(=O)C3=CC=C(C=C3)N

Technology Process of 4-Amino-N-1H-benzimidazol-2-yl-benzenesulfonamide

There total 18 articles about 4-Amino-N-1H-benzimidazol-2-yl-benzenesulfonamide 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: 80.0%

: N-(1,3-dihydrobenzoimidazol-2-ylidene)-4-nitrobenzenesulfonamide

: 52715-11-4
4-amino-N-(1,3-dihydrobenzoimidazol-2-ylidene)benzenesulfonamide

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; for 8h; under 1551.4 Torr;

Reference yield:

: 193696-66-1
4-nitro-benzenesulfonic acid-(1H-benzimidazol-2-ylamide)

: 52715-11-4
sulfanilic acid-(1H-benzimidazol-2-ylamide)

Guidance literature:: With hydrogenchloride; tin;
DOI:10.1093/gerona/56.10.B443

Reference yield:

: 934-32-7
1H-benzimidazol-2-amine

: 52715-11-4
4-amino-N-(1,3-dihydrobenzoimidazol-2-ylidene)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 54.4 percent / pyridine / 18 h / 50 °C

2: 80 percent / H₂ / 5percent Pd/C / ethanol / 8 h / 1551.4 Torr

With pyridine; hydrogen; palladium on activated charcoal; In ethanol;