Dimethyl-[4-(5-nitro-1H-benzoimidazol-2-yl)-phenyl]-amine

Base Information

Chemical Name:Dimethyl-[4-(5-nitro-1H-benzoimidazol-2-yl)-phenyl]-amine
CAS No.:111114-79-5
Molecular Formula:C₁₅H₁₄N₄O₂
Molecular Weight:282.302
Hs Code.:
DSSTox Substance ID:DTXSID401200388
ChEMBL ID:CHEMBL1944803

Synonyms:111114-79-5;n,n-dimethyl-4-(5-nitro-1h-benzo[d]imidazol-2-yl)aniline;Dimethyl-[4-(5-nitro-1H-benzoimidazol-2-yl)-phenyl]-amine;Cambridge id 5822697;Oprea1_143686;Oprea1_480707;SCHEMBL2247164;CHEMBL1944803;DTXSID401200388;AKOS001568027;EU-0033799;AB00098394-01;2-[4-(Dimethylamino)phenyl]-5-nitrobenzimidazole;N,N-Dimethyl-4-(6-nitro-1H-benzimidazol-2-yl)benzenamine

Suppliers and Price of Dimethyl-[4-(5-nitro-1H-benzoimidazol-2-yl)-phenyl]-amine

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 Dimethyl-[4-(5-nitro-1H-benzoimidazol-2-yl)-phenyl]-amine

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:282.11167570
Heavy Atom Count:21
Complexity:376

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CN(C)C1=CC=C(C=C1)C2=NC3=C(N2)C=C(C=C3)[N+](=O)[O-]

Technology Process of Dimethyl-[4-(5-nitro-1H-benzoimidazol-2-yl)-phenyl]-amine

There total 2 articles about Dimethyl-[4-(5-nitro-1H-benzoimidazol-2-yl)-phenyl]-amine 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: 91.0%

: 100-10-7
4-dimethylamino-benzaldehyde

: 99-56-9
4-Nitrophenylene-1,2-diamine

: 111114-79-5
5⁽⁶⁾-nitro-2-(4-(N,N-dimethyl)aminophenyl)-1H-benzimidazole

Guidance literature:: With ferric hydrogen sulphate; In ethanol; at 20 ℃; for 1.33333h; chemoselective reaction;
DOI:10.5012/bkcs.2012.33.2.515