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3,4-diphenyl-5(2H)-isoxazolone is a chemical compound with the molecular formula C15H11NO2. It is a derivative of isoxazolone, featuring two phenyl groups attached to the 3 and 4 positions of the isoxazolone ring. 3,4-diphenyl-5(2H)-isoxazolone is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It can be used as an intermediate in the preparation of biologically active molecules, such as antibiotics and anti-inflammatory agents. The compound is typically synthesized through a cyclization reaction involving a phenylhydrazine derivative and a ketoester, followed by oxidation. Its chemical properties and reactivity make it a valuable building block in organic chemistry and medicinal chemistry research.

957-46-0

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957-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 957-46-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,5 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 957-46:
(5*9)+(4*5)+(3*7)+(2*4)+(1*6)=100
100 % 10 = 0
So 957-46-0 is a valid CAS Registry Number.

957-46-0Relevant academic research and scientific papers

One-Pot Reaction of Carboxylic Acids and Ynol Ethers for the Synthesis of β-Keto Esters

Zeng, Linwei,Lai, Zhencheng,Cui, Sunliang

, p. 14834 - 14841 (2018/12/14)

An one-pot reaction of carboxylic acids and ynol ethers for the synthesis of β-keto esters has been developed. Under promotion of Ag2O, various carboxylic acids and ynol ethers could transform to α-acyloxy enol esters, which undergo a following DMAP-catalyzed rearrangement to deliver β-keto esters rapidly. This method provides a direct approach to β-keto esters from carboxylic acids without any preactivation. The protocol features mild reaction conditions, broad substrate scope, and the products could be transformed to an array of compounds.

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