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1-(2-methoxyphenyl)ethan-1-one O-pivaloyl oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1619224-89-3

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1619224-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1619224-89-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,9,2,2 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1619224-89:
(9*1)+(8*6)+(7*1)+(6*9)+(5*2)+(4*2)+(3*4)+(2*8)+(1*9)=173
173 % 10 = 3
So 1619224-89-3 is a valid CAS Registry Number.

1619224-89-3Relevant academic research and scientific papers

Redox-Neutral Access to Isoquinolinones via Rhodium(III)-Catalyzed Annulations of O-Pivaloyl Oximes with Ketenes

Yang, Xifa,Liu, Song,Yu, Songjie,Kong, Lingheng,Lan, Yu,Li, Xingwei

, p. 2698 - 2701 (2018/05/22)

A mild and redox-neutral [4 + 2] annulation of O-pivaloyl oximes with ketenes has been realized for synthesis of quaternary-carbon-stereocenter-containing (QCSC) isoquinolinones, where the N-OPiv not only acts as an oxidizing group but also offers coordination saturation to inhibit protonolysis. The reaction mechanism has been studied by DFT calculations.

Methyl ketone oxime esters as nucleophilic coupling partners in Pd-catalyzed C-H alkylation and application in the synthesis of isoquinolines

Zhang, Zhi-Wei,Lin, Aijun,Yang, Jiong

, p. 7041 - 7050 (2014/08/18)

Methyl ketone oxime esters have been found to be excellent coupling partners for C(sp2)-C(sp3) bond formation via Pd-catalyzed aromatic C-H activation. This transformation forms the basis of an approach to regioselectively synthesize substituted isoquinolines via coupling with aryloxime esters. Our mechanistic studies suggested that the reaction proceeded through Pd(II)-catalyzed aromatic C-H activation, tautomerization, and a 1,3-shift of the palladacycle-ligated methyl ketone oxime ester to enable the C-C bond formation by reductive elimination, and intramolecular condensation of an imido-Pd(II) intermediate to form the heterocycle. The aryloxime group not only was used as a directing group for Pd-catalyzed aromatic C-H activation but also functioned as an internal oxidant to allow the reaction to be redox-neutral. Our study illuminated the scope and limitations of this C-H alkylation process, which may serve as the point of departure for developing other C-H functionalization reactions using oxime esters and potentially other carbonyl derivatives as the nucleophilic coupling partners.

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