N-cyclohexyl-1H-benzimidazol-2-amine

Base Information

• Chemical Name: N-cyclohexyl-1H-benzimidazol-2-amine
• CAS No.: 83792-76-1
• Molecular Formula: C13H17N3
• Molecular Weight: 215.298
• DSSTox Substance ID: DTXSID30358905
• Nikkaji Number: J1.041.327C
• Wikidata: Q82139818
• Mol file: 83792-76-1.mol

Synonyms:N-cyclohexyl-1H-benzimidazol-2-amine;83792-76-1;N-Cyclohexyl-1H-benzo[d]imidazol-2-amine;N-CYCLOHEXYL-1H-1,3-BENZODIAZOL-2-AMINE;SCHEMBL14155576;DTXSID30358905;MFCD00569561;STL444848;AKOS000283182;1H-benzoimidazol-2-yl-cyclohexyl-amine;LS-06641;CS-0322369

Chemical Property of N-cyclohexyl-1H-benzimidazol-2-amine

Chemical Property:

• XLogP3: 3.4
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 215.142247555
• Heavy Atom Count: 16
• Complexity: 225

Purity/Quality:

99% ^*data from raw suppliers

N-Cyclohexyl-1H-benzimidazol-2-amine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1CCC(CC1)NC2=NC3=CC=CC=C3N2

Technology Process of N-cyclohexyl-1H-benzimidazol-2-amine

There total 12 articles about N-cyclohexyl-1H-benzimidazol-2-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: 99.0%

1-(2-aminophenyl)-3-cyclohexylthiourea (221013-91-8) → (1H-benzoimidazol-2-yl)-(cyclohexyl)-amine (83792-76-1)

Guidance literature:

With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In acetonitrile; at 20 ℃;

DOI:10.1016/j.tetlet.2011.05.146

Reference yield: 85.0%

cyclohexyl isoselenocyanate (4426-69-1) + 1,2-diamino-benzene (95-54-5) → (1H-benzoimidazol-2-yl)-(cyclohexyl)-amine (83792-76-1)

Guidance literature:

In N,N-dimethyl-formamide; at 70 ℃; for 6h;

DOI:10.1055/s-0029-1219395

Reference yield: 84.0%

1H-benzimidazol-2-amine (934-32-7) + cyclohexanol (108-93-0) → (1H-benzoimidazol-2-yl)-(cyclohexyl)-amine (83792-76-1)

Guidance literature:

With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; potassium carbonate; at 130 ℃; for 12h; regioselective reaction;

DOI:10.1002/ejoc.201200698

upstream raw materials:

cyclohexylamine

1-(2-aminophenyl)-3-cyclohexylthiourea

1,2-diamino-benzene

isothiocyanatocyclohexane

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