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2-Phenacyl-4-methylpyridine is an organic compound with the molecular formula C16H13N. It is a derivative of pyridine, featuring a phenacyl group (a phenyl-acyl group) at the 2-position and a methyl group at the 4-position. 2-phenacyl-4-methylpyridine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure. It is typically synthesized through a condensation reaction between 4-methylpyridine and a phenacyl halide or through other organic synthesis routes. The compound is characterized by its aromatic properties and can be further functionalized or used as a building block in the creation of more complex molecules.

3197-57-7

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3197-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3197-57-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,9 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3197-57:
(6*3)+(5*1)+(4*9)+(3*7)+(2*5)+(1*7)=97
97 % 10 = 7
So 3197-57-7 is a valid CAS Registry Number.

3197-57-7Relevant academic research and scientific papers

Solvent free one-pot multi-component synthesis of β-azaarene substituted ketones via a Sn-catalyzed C(sp3)-H functionalization of 2-alkylazaarenes

Chavan, Santosh S.,Pathan, Mohsinkhan Y.,Mulla, Shafeek A. R.

, p. 103091 - 103094 (2015/12/23)

A tin-catalyzed solvent free one-pot multi-component cascade reaction strategy for the direct Michael addition/C(sp3)-H functionalization of 2-alkylazaarenes with aldehydes and ketones via an aldol reaction has been developed. This is the first report and provides cost effective new access to potent biologically/medicinally important azaarene derivatives with high atom economy.

SITE SELECTIVE EFFECT OF N-OXIDE FUNCTION TO METHYL GROUPS ON SIX-MEMBERED N-HETEROAROMATICS

Sakamoto, Takao,Yoshizawa, Hiroshi,Yamanaka, Hiroshi,Goto, Yoshinobu,Niiya, Tokihiro,Honjo, Noriko

, p. 73 - 76 (2007/10/02)

Reaction of 2,4-dimethylpyridine 1-oxide with ethyl benzoate under basic conditions afforded 4-methyl-2-phenacylpyridine 1-oxide, while the same reaction of 2,4-dimethylpyridine itself is known to afford 2-methyl-4-phenacylpyridine.Concerning the above contrast, the effect of N-oxide function to the relative reactivity of the 2- and 4-methyl group was investigated on pyridine, quinoline, pyrimidine, and quinazoline homologues.The higher reactivity of α-methyl groups was concluded to be general in the N-oxides of these N-heteroaromatics.

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