N-1H-Benzimidazol-2-yl-N'-cyclohexyl-N''-(2-methyl-4-quinolinyl)guanidine

Base Information

Chemical Name:N-1H-Benzimidazol-2-yl-N'-cyclohexyl-N''-(2-methyl-4-quinolinyl)guanidine
CAS No.:71080-08-5
Molecular Formula:C₂₄H₂₆N₆
Molecular Weight:398.511
Hs Code.:
DSSTox Substance ID:DTXSID60991405
ChEMBL ID:CHEMBL293738

Synonyms:71080-08-5;Guanidine, 1-(2-benzimidazolyl)-3-cyclohexyl-2-(2-methyl-4-quinolyl)-;N-1H-Benzimidazol-2-yl-N'-cyclohexyl-N''-(2-methyl-4-quinolinyl)guanidine;Guanidine, N-1H-benzimidazol-2-yl-N'-cyclohexyl-N''-(2-methyl-4-quinolinyl)-;CHEMBL293738;DTXSID60991405;3-(1H-benzimidazol-2-yl)-2-cyclohexyl-1-(2-methylquinolin-4-yl)guanidine;LS-73233;N-1H-Benzimidazol-2-yl-N''-cyclohexyl-N'-(2-methylquinolin-4(1H)-ylidene)guanidine

Suppliers and Price of N-1H-Benzimidazol-2-yl-N'-cyclohexyl-N''-(2-methyl-4-quinolinyl)guanidine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-1H-Benzimidazol-2-yl-N'-cyclohexyl-N''-(2-methyl-4-quinolinyl)guanidine

Chemical Property:

Vapor Pressure:4.02E-15mmHg at 25°C
Boiling Point:616.3°C at 760 mmHg
Flash Point:326.5°C
Density:1.31g/cm³
XLogP3:4.9
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:398.22189485
Heavy Atom Count:30
Complexity:588

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=NC2=CC=CC=C2C(=C1)NC(=NC3CCCCC3)NC4=NC5=CC=CC=C5N4

Technology Process of N-1H-Benzimidazol-2-yl-N'-cyclohexyl-N''-(2-methyl-4-quinolinyl)guanidine

There total 3 articles about N-1H-Benzimidazol-2-yl-N'-cyclohexyl-N''-(2-methyl-4-quinolinyl)guanidine 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: 64.0%

: 934-32-7
1H-benzimidazol-2-amine

: 71079-18-0
N¹-cyclohexyl-N²-(2-methyl-4-quinolyl)carbodiimide

: 71080-08-5
N-(1H-benzoimidazol-2-yl)-N'-cyclohexyl-N''-(2-methyl-quinolin-4-yl)-guanidine

Guidance literature:: for 0.5h; Heating;
DOI:10.1021/jm00175a004

Reference yield:

: 71070-70-7
N-cyclohexyl-N'-4-(2-methylquinolyl)urea

: 71080-08-5
N-(1H-benzoimidazol-2-yl)-N'-cyclohexyl-N''-(2-methyl-quinolin-4-yl)-guanidine

Guidance literature:: Multi-step reaction with 2 steps

1: Ph₃P, Et₃N / CCl₄; CH₂Cl₂ / 2 h / Heating

2: 64 percent / 0.5 h / Heating

With triethylamine; triphenylphosphine; In tetrachloromethane; dichloromethane;
DOI:10.1021/jm00175a004