1H-Benzimidazole, 2-(5-((4-nitrophenyl)sulfonyl)-2-furanyl)-

Base Information

Chemical Name:1H-Benzimidazole, 2-(5-((4-nitrophenyl)sulfonyl)-2-furanyl)-
CAS No.:75745-87-8
Molecular Formula:C₁₇H₁₁N₃O₅S
Molecular Weight:369.357
Hs Code.:
DSSTox Substance ID:DTXSID40226646
Wikidata:Q83106130

Synonyms:BRN 4572929;75745-87-8;1H-Benzimidazole, 2-(5-((4-nitrophenyl)sulfonyl)-2-furanyl)-;2-(5-((4-Nitrophenyl)sulfonyl)-2-furanyl)-1H-benzimidazole;C17H11N3O5S;DTXSID40226646;2-{5-[(4-Nitrophenyl)sulfonyl]-2-furyl}-1H-benzimidazole;C17-H11-N3-O5-S;LS-33100

Suppliers and Price of 1H-Benzimidazole, 2-(5-((4-nitrophenyl)sulfonyl)-2-furanyl)-

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-Benzimidazole, 2-(5-((4-nitrophenyl)sulfonyl)-2-furanyl)-

Chemical Property:

Vapor Pressure:3.53E-18mmHg at 25°C
Boiling Point:676.9°Cat760mmHg
Flash Point:363.2°C
Density:1.517g/cm³
XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:369.04194163
Heavy Atom Count:26
Complexity:623

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)NC(=N2)C3=CC=C(O3)S(=O)(=O)C4=CC=C(C=C4)[N+](=O)[O-]

Technology Process of 1H-Benzimidazole, 2-(5-((4-nitrophenyl)sulfonyl)-2-furanyl)-

There total 3 articles about 1H-Benzimidazole, 2-(5-((4-nitrophenyl)sulfonyl)-2-furanyl)- 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: 58.0%

: 5-<(4-nitrophenyl)sulphonyl>-2-furancarboximidate HCl

: 95-54-5
1,2-diamino-benzene

: 75745-87-8
2-<5'-(4''-nitrophenyl)sulphonyl-2'-furanyl>benzimidazole

Guidance literature:: In methanol; for 3h; Ambient temperature;

Reference yield:

: 75745-64-1
5-<(4-nitrophenyl)sulphonyl>-2-furancarbonitrile

: 75745-87-8
2-<5'-(4''-nitrophenyl)sulphonyl-2'-furanyl>benzimidazole

Guidance literature:: Multi-step reaction with 2 steps

1: HCl(g) / 48 h / 0 - 5 °C

2: 58 percent / methanol / 3 h / Ambient temperature

With hydrogenchloride; In methanol;

Reference yield:

: 75745-89-0
5-<(4-nitrophenyl)thio>-2-furancarbonitrile

: 75745-87-8
2-<5'-(4''-nitrophenyl)sulphonyl-2'-furanyl>benzimidazole

Guidance literature:: Multi-step reaction with 3 steps

1: 54 percent / 46percent H₂O₂ / acetic acid / 75 h / Ambient temperature

2: HCl(g) / 48 h / 0 - 5 °C

3: 58 percent / methanol / 3 h / Ambient temperature

With hydrogenchloride; dihydrogen peroxide; In methanol; acetic acid;