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4,6,7,8-tetrahydro-2,4-bis(4-methoxyphenyl)-7,7-dimethyl-5(1H)-quinolinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

130716-57-3

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130716-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130716-57-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,7,1 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 130716-57:
(8*1)+(7*3)+(6*0)+(5*7)+(4*1)+(3*6)+(2*5)+(1*7)=103
103 % 10 = 3
So 130716-57-3 is a valid CAS Registry Number.

130716-57-3Relevant academic research and scientific papers

Regiospecific ring closure reactions of 1, 3-diphenylthiobarbituric acid and dimedone: Formation of spiro vs fused heterocycles

Pati, Anita,Majumdar, Poulomi,Garnayak, Sarita,Behera, Ajaya K.,Behera, Rajani K.

, p. 384 - 391 (2014/05/06)

The one pot reaction of 1, 3-diphenylthiobarbituric acid with benzylidene acetophenone, benzaldehyde and ammonium acetate in presence of catalytic amount of acetic acid furnishes regiospecifically an azaspiro compound. The azaspiro compound has also been

Para substituted benzaldehydes as expedient reagents for the oxidative aromatization of hydroquinoline

Majumdar, Poulomi,Pati, Anita,Behera, Rajani K.,Behera, Ajaya Kumar

, p. 703 - 712 (2013/07/05)

A Cannizzaro-type reaction of tetrahydro-5(1H)-quinolinones with para substituted benzaldehydes in the presence of a base formed the corresponding quinoline and aryl methanol rather than arylidene derivatives because of the oxidation of tetrahydroquinoline and reduction of benzaldehydes as a result of unprecedented hydride transfer from tetrahydroquinoline to arylaldehydes. The reaction proceeds best with the participation of substituents with +M effect in substrate molecule.

A facile and expeditious microwave-assisted synthesis of 4-aryl-2-ferrocenyl-quinoline derivatives via multi-component reaction

Tu, Shu-Jiang,Yan, Shu,Cao, Xu-Dong,Wu, Shan-Shan,Zhang, Xiao-Hong,Hao, Wen-Juan,Han, Zheng-Guo,Shi, Feng

experimental part, p. 91 - 96 (2009/03/12)

An efficient and rapid route for the synthesis of 4-aryl-2-ferrocenyl-quinoline derivatives through microwave-assisted multi-component reaction of acetylferrocene with aromatic aldehyde and dimedone in the presence of ammonium acetate using DMF as reactio

5-OXOHEXAHYDROQUINOLINES, CONDENSED ANALOGS OF 1,4-DIHYDROPYRIDINES. PREPARATION AND PROPERTIES

Kazarinova, T. D.,Markova, L. I.,Kharchenko, V. G.

, p. 438 - 441 (2007/10/02)

The optimum conditions for the preparation of 5-oxohexahydroquinolines have been established, and a probable reaction mechanism for their formation is proposed.Some reactions of these compounds have been examined.

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