4-Methyl-6-phenylpyridin-2(1H)-one

Base Information

Chemical Name:4-Methyl-6-phenylpyridin-2(1H)-one
CAS No.:20364-37-8
Molecular Formula:C12H11NO
Molecular Weight:185.225
Hs Code.:
DSSTox Substance ID:DTXSID90503570
Wikidata:Q82357506

Synonyms:4-Methyl-6-phenylpyridin-2(1H)-one;20364-37-8;SCHEMBL5907056;DTXSID90503570;AKOS006288678

Suppliers and Price of 4-Methyl-6-phenylpyridin-2(1H)-one

Supply Marketing:

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

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Chemical Property of 4-Methyl-6-phenylpyridin-2(1H)-one

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:185.084063974
Heavy Atom Count:14
Complexity:295

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=O)NC(=C1)C2=CC=CC=C2

Technology Process of 4-Methyl-6-phenylpyridin-2(1H)-one

There total 13 articles about 4-Methyl-6-phenylpyridin-2(1H)-one 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: 79.0%

: 487016-54-6
2-chloro-N-(3-oxo-1-phenyl-butyl)-acetamide

: 20364-37-8
4-methyl-6-phenylpyridin-2(1H)-one

Guidance literature:: With tetra-(n-butyl)ammonium iodide; sodium 4-methylbenzenesulfinate; In ethanol; for 6h; Heating;
DOI:10.1023/A:1026146421293

Reference yield: 13.0%

: 5977-14-0
acetoacetamido

: 98-86-2
acetophenone

: 20364-37-8
4-methyl-6-phenylpyridin-2(1H)-one

Guidance literature:: With PPA; at 120 - 125 ℃; for 2h;

Reference yield:

: 52117-38-1
4-phenyl-4-chloro-2-butanone

: 20364-37-8
4-methyl-6-phenylpyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: 56 percent / SnCl₄

2: 79 percent / tetrabutylammonium iodide; sodium p-toluenesulfinate dihydrate / aq. ethanol / 6 h / Heating

With tin(IV) chloride; tetra-(n-butyl)ammonium iodide; sodium 4-methylbenzenesulfinate; In ethanol;
DOI:10.1023/A:1026146421293