6-methyl-2-(4-nitrophenyl)-1H-benzimidazole

Base Information

Chemical Name:6-methyl-2-(4-nitrophenyl)-1H-benzimidazole
CAS No.:69570-93-0
Molecular Formula:C14H11N3O2
Molecular Weight:253.26
Hs Code.:2933990090
DSSTox Substance ID:DTXSID60355260
Nikkaji Number:J2.037.124B
Wikidata:Q82134038
ChEMBL ID:CHEMBL4642399
Mol file:69570-93-0.mol

Synonyms:69570-93-0;6-methyl-2-(4-nitrophenyl)-1H-benzimidazole;CHEMBL4642399;5-methyl-2-(4-nitrophenyl)-1h-benzo[d]imidazole;Cambridge id 5323550;Oprea1_007879;Oprea1_598213;5-METHYL-2-(4-NITROPHENYL)-1H-BENZOIMIDAZOLE;SCHEMBL2250050;DTXSID60355260;PFIPEWJKRTWVRM-UHFFFAOYSA-N;BDBM50541101;AKOS003012608;2-(4-nitrophenyl)-6-methylbenzimidazole;2-(4-nitrophenyl)-6-methyl benzimidazole;5-methyl-2-(4-nitrophenyl)-1 h -benzimidazole;SR-01000514423;SR-01000514423-1

Suppliers and Price of 6-methyl-2-(4-nitrophenyl)-1H-benzimidazole

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

American Custom Chemicals Corporation
5-METHYL-2-(4-NITROPHENYL)-1H-BENZOIMIDAZOLE 95.00%
5MG
$ 501.70

Total 3 raw suppliers

Chemical Property of 6-methyl-2-(4-nitrophenyl)-1H-benzimidazole

Chemical Property:

PSA：74.50000
LogP:3.96970
XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:253.085126602
Heavy Atom Count:19
Complexity:336

Purity/Quality:

≥99% ^*data from raw suppliers

5-METHYL-2-(4-NITROPHENYL)-1H-BENZOIMIDAZOLE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC2=C(C=C1)N=C(N2)C3=CC=C(C=C3)[N+](=O)[O-]

Technology Process of 6-methyl-2-(4-nitrophenyl)-1H-benzimidazole

There total 4 articles about 6-methyl-2-(4-nitrophenyl)-1H-benzimidazole 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: 99.0%

: 555-16-8
4-nitrobenzaldehdye

: 496-72-0
4-methyl-1,2-diaminobenzene

: 69570-93-0
5‐methyl‐2‐(4‐nitrophenyl)‐1H‐benzo[d]imidazole

Guidance literature:: With hydrogenchloride; dihydrogen peroxide; In acetonitrile; at 20 ℃; for 0.833333h;
DOI:10.1055/s-2007-965878

Reference yield: 77.0%

: 39214-83-0
3-(4-nitrophenyl)isoxazol-5(4H)-one

: 496-72-0
4-methyl-1,2-diaminobenzene

: 69570-93-0
5‐methyl‐2‐(4‐nitrophenyl)‐1H‐benzo[d]imidazole

: 139436-63-8
6-Methyl-2-(4-nitro-phenyl)-quinoxaline

Guidance literature:: In acetonitrile; Heating;

Reference yield: 73.0%

: 29289-13-2
2-iodo-4-methylaniline

: 15723-90-7
4-nitrobenzamidine hydrochloride

: 69570-93-0
5‐methyl‐2‐(4‐nitrophenyl)‐1H‐benzo[d]imidazole

Guidance literature:: With copper(I) oxide; caesium carbonate; N,N`-dimethylethylenediamine; In N,N-dimethyl-formamide; at 140 ℃; for 16h; Inert atmosphere;
DOI:10.1016/j.tet.2012.12.039