1,3-Diisopropylbenzimidazolium bromide

Base Information

Chemical Name:1,3-Diisopropylbenzimidazolium bromide
CAS No.:684283-51-0
Molecular Formula:C13H19N2.Br
Molecular Weight:283.211
Hs Code.:
European Community (EC) Number:878-592-2

Synonyms:684283-51-0;1,3-diisopropylbenzimidazolium bromide;1,3-Diisopropyl-1H-benzo[d]imidazol-3-ium bromide;MFCD33398687;1,3-di(propan-2-yl)benzimidazol-3-ium;bromide;starbld0029044;BS-48219;SY318901;1,3-Diisopropylbenzimidazol-3-ium Bromide;D5778;F72009

Suppliers and Price of 1,3-Diisopropylbenzimidazolium bromide

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 7 raw suppliers

Chemical Property of 1,3-Diisopropylbenzimidazolium bromide

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:282.07316
Heavy Atom Count:16
Complexity:191

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)N1C=[N+](C2=CC=CC=C21)C(C)C.[Br-]

Technology Process of 1,3-Diisopropylbenzimidazolium bromide

There total 5 articles about 1,3-Diisopropylbenzimidazolium bromide 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: 86.0%

: 51-17-2,79351-71-6
benzoimidazole

: 75-26-3
isopropyl bromide

: 684283-51-0
1,3-diisopropyl-1H-benzo[d]imidazol-3-ium bromide

Guidance literature:: benzoimidazole; With potassium carbonate; In acetonitrile; at 20 ℃; for 1h; Inert atmosphere;

isopropyl bromide; In acetonitrile; for 96h; Reflux; Inert atmosphere;
DOI:10.1002/anie.202106142

Reference yield: 31.0%

: 17583-50-5
N-isopropylbenzimidazole

: 75-26-3
isopropyl bromide

: 684283-51-0
1,3-diisopropyl-1H-benzo[d]imidazol-3-ium bromide

Guidance literature:: In toluene; for 26h;
DOI:10.1023/B:RUJO.0000010563.79902.47

Reference yield:

: 51-17-2,79351-71-6
benzoimidazole

: 684283-51-0
1,3-diisopropyl-1H-benzo[d]imidazol-3-ium bromide

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / potassium hydroxide / dimethylsulfoxide / 2 h / 18 - 20 °C

2: 31 percent / toluene / 26 h

With potassium hydroxide; In dimethyl sulfoxide; toluene;
DOI:10.1023/B:RUJO.0000010563.79902.47