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3-ethoxalyl-5,6,7,8-tetrafluoro-1-(2-methylphenyl)-1,4-dihydroquinolin-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

312928-17-9

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312928-17-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 312928-17-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,2,9,2 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 312928-17:
(8*3)+(7*1)+(6*2)+(5*9)+(4*2)+(3*8)+(2*1)+(1*7)=129
129 % 10 = 9
So 312928-17-9 is a valid CAS Registry Number.

312928-17-9Relevant academic research and scientific papers

Synthesis of 2-(1-alkyl(aryl)-4-oxo-5,6,7,8-tetrafluoro-1,4-dihydroquinolin-3-yl)glyoxylic acid derivatives

Fokin,Burgart,Saloutin,Chupakhin

, p. 187 - 194 (2007/10/03)

Methods for synthesis of previously unknown 2-(1-alkyl(aryl)-4-oxo-5,6,7,8-tetrafluoro-1,4-dihydroquinolin-3-yl)glyoxylic acids and their esters from the copper chelate of ethyl pentafluorobenzoylpyruvate were developed. 1-Aryl(alkyl)-3-ethoxalyl-5,6,7,8-tetrafluoro-quinolin-4-ones react with o-phenylenediamine and o-aminophenol to give the corresponding quinolin-3-ylquinoxalones and quinolin-3-ylbenzoxazines. The same heterocycles act with o-aminothiophenol to yield ethyl-2-(7-(2-aminophenylthio)-1-aryl-5,6,8-trifluoro-quinolon-3-yl)-2- (2-mercaptophenylimino)glioxylates. Interaction of 1-aryl-3-ethoxalyl-(heteryl)-5,6,7,8-tetrafluoroquinolones with morpholine gives 7-mono- and 5,7-disubstituted products depending on the reaction conditions.

Synthesis of N-substituted 2-(5,6,7,8-tetrafluoro-4-oxo-1,4-dihydroquinolin-3-yl)glyoxylic acids

Obanin,Fokin,Burgart,Ryzhkov,Skryabina,Saloutin,Chupakhin

, p. 1231 - 1236 (2007/10/03)

Methods for the synthesis of the earlier unknown N-substituted 2-(5,6,7,8-tetrafluoro-4-oxo-1,4-dihydroquinolin-3-yl)glyoxylic acids and their esters from copper chelate of ethyl pentafluorobenzoylpyruvate were developed. The structure of intermediate ethyl 4-(R-amino)-2-oxo-3-pentafluorobenzoylbut-3-enoates is discussed.

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