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2-oxo-3-(pyridin-2-yl)-2H-chromen-7-yl acetate is a complex organic compound with the molecular formula C17H11NO4. It is a derivative of the flavonoid family, characterized by a 2-oxo-2H-chromene core structure, which includes a pyridin-2-yl group at the 3-position and an acetate group at the 7-position. 2-oxo-3-(pyridin-2-yl)-2H-chromen-7-yl acetate is known for its potential biological activities, such as antioxidant and anti-inflammatory properties, and is often studied for its role in pharmaceutical research. It is synthesized through a series of chemical reactions and is typically found in a crystalline form. The compound's structure and properties make it a subject of interest in the development of new drugs and therapeutic agents.

1157-93-3

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1157-93-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1157-93-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,5 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1157-93:
(6*1)+(5*1)+(4*5)+(3*7)+(2*9)+(1*3)=73
73 % 10 = 3
So 1157-93-3 is a valid CAS Registry Number.

1157-93-3Downstream Products

1157-93-3Relevant academic research and scientific papers

3-(2-Pyridyl)coumarins

Khilya,Shablykina,Frasinyuk,Ishchenko,Khilya

, p. 523 - 528 (2005)

3-(2-Pyridyl)coumarins were prepared by reaction of substituted salicylaldehydes and 2-pyridylacetonitrile. Benzylation, acylation, and aminomethylation of 7-hydroxy-3-(2-pyridyl)coumarin was studied. 2005 Springer Science+Business Media, Inc.

Syntheses, Absorption and Fluorescence Spectra of 7-Hydroxy-3-pyridylcoumarins, their Esters, Ethers, and Quaternized Derivatives

Wolfbeis, Otto S.,Marhold, Harry

, p. 3664 - 3672 (2007/10/02)

7-Hydroxycoumarins 4 with a 2-, 3- or 4-pyridyl substituent in position 3, their ethers (3), esters (5, 6), and quaternized derivatives (7-9) have been synthesized by a generally applicable method starting from 2-hydroxy-4-methoxybenzaldehyde (1).The absorption and fluorescence spectra in methanol and water of different pH values are reported, and the effects of substituents on spectra and pKa values are discussed.

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