N-cyclohexyl-4,5-diphenyl-1,3-thiazol-2-amine

Base Information

• Chemical Name: N-cyclohexyl-4,5-diphenyl-1,3-thiazol-2-amine
• CAS No.: 122641-43-4
• Molecular Formula: C21H22N2S
• Molecular Weight: 334.47800
• DSSTox Substance ID: DTXSID60365167
• Nikkaji Number: J1.693.074A
• Wikidata: Q82149616
• Mol file: 122641-43-4.mol

Synonyms:N-cyclohexyl-4,5-diphenyl-1,3-thiazol-2-amine;122641-43-4;2-Thiazolamine, N-cyclohexyl-4,5-diphenyl-;Oprea1_790817;DTXSID60365167;N-Cyclohexyl-4,5-diphenylthiazole-2-amine;AI-020/37280046;Z48858397

Chemical Property of N-cyclohexyl-4,5-diphenyl-1,3-thiazol-2-amine

Chemical Property:

• PSA: 56.39000
• LogP: 5.64360
• XLogP3: 6.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 334.15036988
• Heavy Atom Count: 24
• Complexity: 370

Purity/Quality:

N-CYCLOHEXYL-4,5-DIPHENYL-1,3-THIAZOL-2-AMINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCC(CC1)NC2=NC(=C(S2)C3=CC=CC=C3)C4=CC=CC=C4

Technology Process of N-cyclohexyl-4,5-diphenyl-1,3-thiazol-2-amine

There total 2 articles about N-cyclohexyl-4,5-diphenyl-1,3-thiazol-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: 95.0%

potassium thioacyanate (333-20-0) + cyclohexylamine (108-91-8,157973-60-9) + desyl bromide (1484-50-0) → 2-cyclo-hexylamino-4,5-diphenylthiazole (122641-43-4)

Guidance literature:

With ammonium acetate on neutral alumina; silica gel; In benzene; at 80 ℃; for 6h;

DOI:10.1016/S0040-4039(02)00084-9

Reference yield: 95.0%

potassium thioacyanate (333-20-0) + cyclohexylammonium acetate (7346-79-4) + desyl bromide (1484-50-0) → 2-cyclo-hexylamino-4,5-diphenylthiazole (122641-43-4)

Guidance literature:

With aluminum oxide; silica gel; In benzene; at 80 ℃; for 6h;

DOI:10.1016/j.tet.2006.01.075

upstream raw materials:

potassium thioacyanate

cyclohexylamine

desyl bromide

cyclohexylammonium acetate