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γ-Methyl-γ-p-tolyl-vinylacetic acid is a complex organic compound with the chemical formula C13H14O2. It is a derivative of vinylacetic acid, featuring a methyl group (-CH3) and a p-tolyl group (a phenyl ring with a methyl substituent at the para position) attached to the γ-carbon. This molecule is of interest in organic chemistry and may have potential applications in the synthesis of various pharmaceuticals and other chemical products due to its unique structural features. The compound's specific properties and reactivity can be influenced by the presence of these substituents, making it a subject of study for its potential roles in chemical reactions and its ability to form derivatives.

16020-19-2

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16020-19-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16020-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,2 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16020-19:
(7*1)+(6*6)+(5*0)+(4*2)+(3*0)+(2*1)+(1*9)=62
62 % 10 = 2
So 16020-19-2 is a valid CAS Registry Number.

16020-19-2Relevant academic research and scientific papers

Copper-catalyzed vinylogous aerobic oxidation of unsaturated compounds with air

Zhang, Hai-Jun,Schuppe, Alexander W.,Pan, Shi-Tao,Chen, Jin-Xiang,Wang, Bo-Ran,Newhouse, Timothy R.,Yin, Liang

, p. 5300 - 5310 (2018/04/24)

A mild and operationally simple copper-catalyzed vinylogous aerobic oxidation of β,γ- and α,β-unsaturated esters is described. This method features good yields, broad substrate scope, excellent chemo- and regioselectivity, and good functional group tolerance. This method is additionally capable of oxidizing β,γ- and α,β-unsaturated aldehydes, ketones, amides, nitriles, and sulfones. Furthermore, the present catalytic system is suitable for bisvinylogous and trisvinylogous oxidation. Tetramethylguanidine (TMG) was found to be crucial in its role as a base, but we also speculate that it serves as a ligand to copper(II) triflate to produce the active copper(II) catalyst. Mechanistic experiments conducted suggest a plausible reaction pathway via an allylcopper(II) species. Finally, the breadth of scope and power of this methodology are demonstrated through its application to complex natural product substrates.

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