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2-(2-bromo-4,5-dimethoxyphenyl)-2-methylpropanenitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

501662-79-9

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501662-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501662-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,6,6 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 501662-79:
(8*5)+(7*0)+(6*1)+(5*6)+(4*6)+(3*2)+(2*7)+(1*9)=129
129 % 10 = 9
So 501662-79-9 is a valid CAS Registry Number.

501662-79-9Relevant academic research and scientific papers

Diastereoselective Construction of Eight-Membered Carbocycles through Palladium-Catalyzed C(sp3)-H Functionalization

Wan, Bin,Lu, Zhuoer,Wu, Zhuo,Cheng, Cang,Zhang, Yanghui

supporting information, p. 1269 - 1274 (2021/03/03)

A palladium-catalyzed cross-coupling reaction of 2-alkylphenyl bromides with biphenylene has been developed. The reactions formed eight-membered carbocycles through C(sp3)-H activation and the formation of two C-C bonds, and the chiral products were obtai

Synthesis of Amides and Esters by Palladium(0)-Catalyzed Carbonylative C(sp3)?H Activation

?arny, Tomá?,Baudoin, Olivier,Clemenceau, Antonin,Rocaboy, Ronan

supporting information, p. 18980 - 18984 (2020/09/01)

The 1,4-palladium shift strategy allows the functionalization of remote C?H bonds that are difficult to reach directly. Reported here is a domino reaction proceeding by C(sp3)?H activation, 1,4-palladium shift, and amino- or alkoxycarbonylation, which generates a variety of amides and esters bearing a quaternary β-carbon atom. Mechanistic studies showed that the aminocarbonylation of the σ-alkylpalladium intermediate arising from the palladium shift is fast using PPh3 as the ligand, and leads to the amide rather than the previously reported indanone product.

Fe-catalyzed regiodivergent [1,2]-shift of α-aryl aldehydes

Gutierrez-Bonet, Alvaro,Flores-Gaspar, Areli,Martin, Ruben

supporting information, p. 12576 - 12579 (2013/09/23)

An Fe-catalyzed conversion of aldehydes to ketones via [1,2]-shift has been developed. This skeletal rearrangement shows a wide substrate scope and chemoselectivity profile while exhibiting an excellent [1,2]-aryl or [1,2]-alkyl shift selectivity that is easily switched by electronic effects.

Pd-catalyzed intramolecular acylation of aryl bromides via C-H functionalization: A highly efficient synthesis of benzocyclobutenones

Alvarez-Bercedo, Paula,Flores-Gaspar, Areli,Correa, Arkaitz,Martin, Ruben

supporting information; experimental part, p. 466 - 467 (2010/03/25)

(Chemical Equation Presented) A new catalyst system for the intramolecular acylation of aldehydes with aryl bromides via C-H functionalization is described. The transformation is distinguished by a remarkable functional group tolerance and hence allows fo

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