alpha-(1-Methyl-2-phenyl-1H-imidazol-4-yl)-4-morpholineacetonitrile

Base Information

Chemical Name:alpha-(1-Methyl-2-phenyl-1H-imidazol-4-yl)-4-morpholineacetonitrile
CAS No.:94938-04-2
Molecular Formula:C₁₆H₁₈N₄O
Molecular Weight:282.345
Hs Code.:
DSSTox Substance ID:DTXSID801174197

Synonyms:SCHEMBL10654721;DTXSID801174197;alpha-(1-Methyl-2-phenyl-1H-imidazol-4-yl)-4-morpholineacetonitrile;94938-04-2

Suppliers and Price of alpha-(1-Methyl-2-phenyl-1H-imidazol-4-yl)-4-morpholineacetonitrile

Supply Marketing:

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

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Chemical Property of alpha-(1-Methyl-2-phenyl-1H-imidazol-4-yl)-4-morpholineacetonitrile

Chemical Property:

XLogP3:1.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:282.14806121
Heavy Atom Count:21
Complexity:381

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CN1C=C(N=C1C2=CC=CC=C2)C(C#N)N3CCOCC3

Technology Process of alpha-(1-Methyl-2-phenyl-1H-imidazol-4-yl)-4-morpholineacetonitrile

There total 1 articles about alpha-(1-Methyl-2-phenyl-1H-imidazol-4-yl)-4-morpholineacetonitrile 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:

: 110-91-8,99108-56-2
morpholine

: 151-50-8
potassium cyanide

: 68282-47-3
2-phenyl-1H-imidazole-4-carbaldehyde

: 74-88-4
methyl iodide

: 94938-04-2
α-(1-methyl-2-phenyl-1H-imidazol-4-yl)-4-morpholineacetonitrile

: 94938-05-3
α-(1-methyl-2-phenyl-1H-imidazol-5-yl)-4-morpholineacetonitrile

Guidance literature:: With sodium methylate; toluene-4-sulfonic acid; Multistep reaction. Title compound not separated from byproducts; 1.) DMF, 23 deg C, 6 h, 2.) dioxane, reflux, 1.5 h;
DOI:10.1021/jm00152a015