1-Trityl-4-(2,2-diphenylethyl)-5-methylimidazole

Base Information

Chemical Name:1-Trityl-4-(2,2-diphenylethyl)-5-methylimidazole
CAS No.:106147-86-8
Molecular Formula:C₃₇H₃₂N₂
Molecular Weight:504.674
Hs Code.:
DSSTox Substance ID:DTXSID601175749

Synonyms:1-trityl-4-(2,2-diphenylethyl)-5-methylimidazole;SCHEMBL10457156;MTOGRKZPJQVAMC-UHFFFAOYSA-N;DTXSID601175749;106147-86-8;4-(2,2-Diphenylethyl)-5-methyl-1-(triphenylmethyl)-1H-imidazole

Suppliers and Price of 1-Trityl-4-(2,2-diphenylethyl)-5-methylimidazole

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
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Total 0 raw suppliers

Chemical Property of 1-Trityl-4-(2,2-diphenylethyl)-5-methylimidazole

Chemical Property:

XLogP3:8.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:8
Exact Mass:504.256549029
Heavy Atom Count:39
Complexity:639

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(N=CN1C(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)CC(C5=CC=CC=C5)C6=CC=CC=C6

Technology Process of 1-Trityl-4-(2,2-diphenylethyl)-5-methylimidazole

There total 4 articles about 1-Trityl-4-(2,2-diphenylethyl)-5-methylimidazole 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:

: 76-83-5
trityl chloride

: 106147-86-8
4-(2,2-diphenylethyl)-5-methyl-1-tritylimidazole

Guidance literature:: Multi-step reaction with 3 steps

1: 10 percent / triethylamine / dimethylformamide / 16 h / Ambient temperature

2: thionyl chloride, triethylamine / benzene / 0.75 h / Ambient temperature

With thionyl chloride; triethylamine; In N,N-dimethyl-formamide; benzene;
DOI:10.1016/0223-5234(90)90180-B

Reference yield:

: 106147-84-6
4-Hydroxymethyl-5-methyl-1-(triphenylmethyl)imidazole

: 106147-86-8
4-(2,2-diphenylethyl)-5-methyl-1-tritylimidazole

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride, triethylamine / benzene / 0.75 h / Ambient temperature

With thionyl chloride; triethylamine; In benzene;
DOI:10.1016/0223-5234(90)90180-B

Reference yield:

: 29636-87-1
4⁽⁵⁾-methyl-5⁽⁴⁾-hydroxymethylimidazole

: 106147-86-8
4-(2,2-diphenylethyl)-5-methyl-1-tritylimidazole

Guidance literature:: Multi-step reaction with 3 steps

1: 10 percent / triethylamine / dimethylformamide / 16 h / Ambient temperature

2: thionyl chloride, triethylamine / benzene / 0.75 h / Ambient temperature

With thionyl chloride; triethylamine; In N,N-dimethyl-formamide; benzene;
DOI:10.1016/0223-5234(90)90180-B