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ethyl 2-(2-chlorophenyl)-2-phenylacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22490-01-3

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22490-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22490-01-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,9 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 22490-01:
(7*2)+(6*2)+(5*4)+(4*9)+(3*0)+(2*0)+(1*1)=83
83 % 10 = 3
So 22490-01-3 is a valid CAS Registry Number.

22490-01-3Downstream Products

22490-01-3Relevant academic research and scientific papers

Catalytic C-C coupling of diazo compounds with arylboronic acids: Using surface modified sewage sludge as catalyst

Huang, Fei,Huang, He,Hughes, Timothy,Xie, Yuxing,Xu, Jun,Yu, Yang,Zhang, Zhipeng

, p. 4165 - 4173 (2020/07/14)

A green, mild and efficient synthesis of diarylmethines using sewage sludge-derived carbonaceous materials (SW) by perchloric acid catalyzed coupling reactions between diazo compounds and arylboronic acids was developed. The reaction shows a high level of functional tolerance and a broad substrate scope. Furthermore, the highly selective 1,2-alkyl shift products were furnished through the sterically demanding R4, R5 migration of diazo compounds (3-diazochromanone). The structures of 1,2-shift products have been further confirmed by single-crystal X-ray analysis. Significantly, the synthesis of the core structures of darifenacin (a clinical drug for overactive bladder syndrome, OAB) and diclofensine (a stimulant drug showing antidepressant and monoamine reuptake inhibitor activity) further demonstrated the efficacy and synthetic potential of this method. This journal is

Synthesis of chiral α-diarylacetic esters by stereospecific 1,2-aryl migration promoted by in situ generated acetals from benzoins

Kothapalli, Raveendra Babu,Niddana, Ramana,Balamurugan, Rengarajan

supporting information, p. 1278 - 1281 (2014/04/03)

A simple protocol for the synthesis of α-diarylacetic esters from benzoins is described. In situ generated acetal assists rapid 1,2-aryl migration in a stereospecific manner, paving the way to make enantioenriched α-diarylacetic esters from easily accessi

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