1-Methylbenzimidazole-2-carboximidamide

Base Information

Chemical Name:1-Methylbenzimidazole-2-carboximidamide
CAS No.:69006-95-7
Molecular Formula:C9H10N4
Molecular Weight:174.2025
Hs Code.:
DSSTox Substance ID:DTXSID701261062
Nikkaji Number:J982.883D
Mol file:69006-95-7.mol

Synonyms:69006-95-7;DTXSID701261062;1-Methyl-1H-benzimidazole-2-carboximidamide

Suppliers and Price of 1-Methylbenzimidazole-2-carboximidamide

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 3 raw suppliers

Chemical Property of 1-Methylbenzimidazole-2-carboximidamide

Chemical Property:

XLogP3:0.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:174.090546336
Heavy Atom Count:13
Complexity:216

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CN1C2=CC=CC=C2N=C1C(=N)N

Technology Process of 1-Methylbenzimidazole-2-carboximidamide

There total 3 articles about 1-Methylbenzimidazole-2-carboximidamide 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: 67.0%

: 105391-94-4
1-Methyl-1H-benzoimidazole-2-carbodithioic acid methyl ester

: 69006-95-7
1-methyl-1H-benzoimidazole-2-carboximidic acid amide

Guidance literature:: With ammonia; sodium methylate; In methanol; at 80 ℃; for 24h; sealed tube;
DOI:10.1016/S0040-4039(98)01222-2

Reference yield:

: 1632-83-3
1-Methylbenzimidazole

: 69006-95-7
1-methyl-1H-benzoimidazole-2-carboximidic acid amide

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) n-BuLi / 1.) THF, -78 deg C; 2.) r.t.

2: 67 percent / NH₃, NaOMe / methanol / 24 h / 80 °C / sealed tube

With n-butyllithium; ammonia; sodium methylate; In methanol;
DOI:10.1016/S0040-4039(98)01222-2