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(Z)-ethyl 3-((3,5-dimethoxyphenyl)amino)-2-(4-methoxyphenyl)acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

190774-07-3

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190774-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 190774-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,7,7 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 190774-07:
(8*1)+(7*9)+(6*0)+(5*7)+(4*7)+(3*4)+(2*0)+(1*7)=153
153 % 10 = 3
So 190774-07-3 is a valid CAS Registry Number.

190774-07-3Relevant articles and documents

Synthesis, structure, and structure-activity relationship analysis of enamines as potential antibacterials

Xiao, Zhu-Ping,Xue, Jia-Yu,Tan, Shu-Hua,Li, Huan-Qiu,Zhu, Hai-Liang

, p. 4212 - 4219 (2007)

Twenty-four enamines were synthesized and reported for the first time. Their chemical structures were confirmed by means of 1H NMR, ESI mass spectra, and elemental analyses, and four of them were determined by single crystal X-ray diffraction a

Synthesis and anticancer evaluation of 3-substituted quinolin-4-ones and 2,3-dihydroquinolin-4-ones

Rajput, Santosh,Gardner, Christopher R.,Failes, Timothy W.,Arndt, Greg M.,Black, David Stc.,Kumar, Naresh

, p. 105 - 115 (2014/01/17)

A series of 3-aryl-5,7-dimethoxyquinolin-4-ones 8 and 3-aryl-5,7-dimethoxy- 2,3-dihydroquinolin-4-ones 13 were synthesized in good yields. Demethylation under a range of conditions afforded the corresponding 5-hydroxy and 5,7-dihydroxy derivatives. Biolog

Synthesis of 3-(4-methoxyphenyl)-5,7-dimethoxy-(1H)-quinolin-2- or 4-ones and derivatives

Croisy, Martine,Huel, Christiane,Bisagni, Emile

, p. 683 - 690 (2007/10/03)

Condensation of ethyl 2-(4-methoxyphenyl)-3-hydroxyacrylate with 3,5-dimethoxyaniline afforded, depending on experimental conditions, either 3-(4-methoxyphenyl)-5,7-dimethoxy-(1H)-quinolin-2-one or 3-(4-methoxyphenyl)-5,7-dimethoxy-(1H)-quinolin-4-one. Whereas chlorination with phosphorous oxychloride led to the corresponding 2- and 4- chloroquinolines derivatives, 2-chloro-3-(4-methoxyphenyl)-5,7-dimethoxyquinoline was also obtained by using the Meth Cohn method's.

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