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53774-19-9

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53774-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53774-19-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,7 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53774-19:
(7*5)+(6*3)+(5*7)+(4*7)+(3*4)+(2*1)+(1*9)=139
139 % 10 = 9
So 53774-19-9 is a valid CAS Registry Number.

53774-19-9Relevant articles and documents

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

supporting information, 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.

Use of formate salts as a hydride and a Co2 source in PGeP -palladium complex-catalyzed hydrocarboxylation of allenes

Zhu, Chuan,Takaya, Jun,Iwasawa, Nobuharu

supporting information, p. 1814 - 1817 (2015/04/14)

Use of formate salts as a hydride as well as a CO2 source was achieved in a PGeP-palladium complex-catalyzed hydrocarboxylation of allenes through a highly efficient decarboxylation-carboxylation process. This reaction proceeds under mild conditions and provides an alternative strategy for utilizing formate salts as a C1 source.

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