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methyl 2-(2-aminophenyl)cyclopent-1-ene carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52909-79-2

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52909-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52909-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,9,0 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52909-79:
(7*5)+(6*2)+(5*9)+(4*0)+(3*9)+(2*7)+(1*9)=142
142 % 10 = 2
So 52909-79-2 is a valid CAS Registry Number.

52909-79-2Downstream Products

52909-79-2Relevant academic research and scientific papers

A simple and fast synthetic pathway of β-Enamino-esters by condensation of β-Keto ester with aliphatic and aromatic amines in ethanol

Kouadri,Ouahrani,Missaoui,Chebrouk,Gherraf

, p. 2575 - 2578 (2015)

The β-keto ester undergoes condensation reactions with aliphatic and aromatic amines in ethanol to give high-yielding β-enamino ester. The method is simple, cost-effective and environmentally benign. Structural characterization of the synthesized compound

Silica Gel-mediated Synthesis of β-Enamino Esters and its Application for the Synthesis of Indeno 4-Hydroxypyridin-2(1H)-Ones

Kim, Soong-Hyun,Bae, Seri,Ko, Eun Bi,Park, Ga Young,Lee, Eunhye,Hwang, Hee Jong,Im, Chun Young,Song, Minsoo

, p. 262 - 269 (2019/02/09)

The full scope of SiO2-based condensation of aliphatic or aromatic amines and β-keto esters to give β-enamino esters was examined. Functionalized linear β-enamino esters were easily obtained from SiO2-based condensation of β-keto esters and amines only after simple filtration. It was also demonstrated that cyclic β-enamino esters with 99% purity can be prepared in a practically large scale (60 g) without using silica gel column chromatography. The utility of the present method was fortified by the preparation of pharmaceutically useful indeno-4-hydroxypyridin-2(1H)-one analogue 11.

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