4,5-diphenyl-2-propyl-1H-imidazole

Base Information

Chemical Name:4,5-diphenyl-2-propyl-1H-imidazole
CAS No.:74181-31-0
Molecular Formula:C₁₈H₁₈N₂
Molecular Weight:262.354
Hs Code.:
European Community (EC) Number:635-114-5
Nikkaji Number:J2.567.165A

Synonyms:4,5-diphenyl-2-propyl-1H-imidazole;74181-31-0;SCHEMBL9518314;2-propyl-4,5-diphenylimidazole;AKOS024332226;4,5-DIPHENYL-2-PROPYLIMIDAZOLE

Suppliers and Price of 4,5-diphenyl-2-propyl-1H-imidazole

Supply Marketing:

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

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Chemical Property of 4,5-diphenyl-2-propyl-1H-imidazole

Chemical Property:

XLogP3:4.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:262.146998583
Heavy Atom Count:20
Complexity:279

Purity/Quality:

Safty Information:

Pictogram(s):
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MSDS Files:

Useful:

Canonical SMILES:CCCC1=NC(=C(N1)C2=CC=CC=C2)C3=CC=CC=C3

Technology Process of 4,5-diphenyl-2-propyl-1H-imidazole

There total 7 articles about 4,5-diphenyl-2-propyl-1H-imidazole 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: 93.0%

: 119-53-9,579-44-2
2-hydroxy-2-phenylacetophenone

: 123-72-8
butyraldehyde

: 74181-31-0
2-n-propyl-4,5-diphenyl-1H-imidazole

Guidance literature:: With ammonium acetate; at 20 ℃; for 0.3h;
DOI:10.1016/j.jorganchem.2018.07.008

Reference yield: 91.0%

: 123-72-8
butyraldehyde

: 134-81-6
benzil

: 74181-31-0
2-n-propyl-4,5-diphenyl-1H-imidazole

Guidance literature:: With 1-hexyl-3-methyl-1H-imidazol-3-ium trifluoroacetate; ammonium acetate; In water; at 80 ℃; for 1h; Green chemistry;
DOI:10.1016/j.tetlet.2013.03.008