10420-97-0 Usage
Description
1-(4-methoxyphenyl)-2-(pyridin-2-yl)ethanone, also known as 4'-Methoxy-2-pyridylacetophenone, is a chemical compound with the molecular formula C15H13NO2. It is a yellow solid at room temperature, soluble in organic solvents like ethanol and acetone, and is widely utilized as a reagent in organic synthesis. 1-(4-methoxyphenyl)-2-(pyridin-2-yl)ethanone is also recognized for its aromatic properties and is commonly used in the production of pharmaceuticals, agrochemicals, and other fine chemicals.
Uses
Used in Pharmaceutical Industry:
1-(4-methoxyphenyl)-2-(pyridin-2-yl)ethanone is used as a reagent for the synthesis of various pharmaceutical compounds due to its versatile chemical structure and solubility in organic solvents. Its ability to interact with other molecules makes it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(4-methoxyphenyl)-2-(pyridin-2-yl)ethanone is used as a reagent in the synthesis of agrochemicals, contributing to the development of pesticides and other products that aid in crop protection and enhancement.
Used in Organic Synthesis:
As a reagent in organic synthesis, 1-(4-methoxyphenyl)-2-(pyridin-2-yl)ethanone is used for the production of a wide range of fine chemicals. Its aromatic properties and solubility in organic solvents make it a preferred choice for various chemical reactions and the creation of complex molecular structures.
Used as an Intermediate:
1-(4-methoxyphenyl)-2-(pyridin-2-yl)ethanone is also used as an intermediate in the synthesis of other compounds, highlighting its importance in the chemical industry for creating a diverse array of products.
Check Digit Verification of cas no
The CAS Registry Mumber 10420-97-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,2 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10420-97:
(7*1)+(6*0)+(5*4)+(4*2)+(3*0)+(2*9)+(1*7)=60
60 % 10 = 0
So 10420-97-0 is a valid CAS Registry Number.
10420-97-0Relevant articles and documents
Tautomer-selective derivatives of enolate, ketone and enaminone by addition reaction of picolyl-type anions with nitriles
Bai, Jianliang,Wang, Peng,Cao, Wei,Chen, Xia
, p. 645 - 652 (2017)
We describe an efficient for the synthesis of compounds of tautomeric β-pyridyl/quinolyl-enol, -ketone, -enaminone, which were finally characterized by standard methods like NMR, IR or SCXRD. The addition reaction of lithiated intermediates of picoline, 2-ethylpyridine and 2-methylquinoline, respectively, with nitriles followed by acid hydrolysis afforded the corresponding tautomeric compounds of enol, ketone and emaminone. Interestingly, treatment of 2-methylpyridine or 2-ethylpyridine with nitriles, respectively, yielded mostly β-pyridyl ketone and enol tautomers without enaminones, while 2-methylquinoline with nitriles gave β-quinolyl ketone and enaminone tautomers without enols. The reaction of 2-benzylpyridine with nitriles was not available under the same conditions.
Catalytic α-Arylation of Ketones with Heteroaromatic Esters
Isshiki, Ryota,Takise, Ryosuke,Itami, Kenichiro,Muto, Kei,Yamaguchi, Junichiro
supporting information, p. 2599 - 2603 (2017/10/31)
Heteroaromatic esters were found to be applicable as an arylating agent for the Pd-catalyzed α-arylation of ketones in a decarbonylative fashion. The use of our in-house ligand, dcypt, enabled this unique bond formation. Considering the ubiquity and low cost of aromatic esters, the present work will allow for rapid access to valuable α-aryl carbonyl compounds.
Synthesis and biological activities of 4-phenyl-5-pyridyl-1,3-thiazole derivatives as selective adenosine A3 antagonists
Miwatashi, Seiji,Arikawa, Yasuyoshi,Matsumoto, Tatsumi,Uga, Keiko,Kanzaki, Naoyuki,Imai, Yumi N.,Ohkawa, Shigenori
experimental part, p. 1126 - 1137 (2009/09/25)
To investigate the potency of an adenosine A3 receptor (A 3AR) antagonist as an anti-asthmatic drug, a novel series of 4-phenyl-5-pyridyl-1,3-thiazole derivatives was synthesized and evaluated in human adenosine A1, A