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1-bromo-2-(4-methoxyphenethyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

937634-53-2

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937634-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 937634-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,7,6,3 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 937634-53:
(8*9)+(7*3)+(6*7)+(5*6)+(4*3)+(3*4)+(2*5)+(1*3)=202
202 % 10 = 2
So 937634-53-2 is a valid CAS Registry Number.

937634-53-2Downstream Products

937634-53-2Relevant academic research and scientific papers

Catalytic Asymmetric Synthesis of Atropisomeric Quinolines through the Friedl?nder Reaction

Hu, Xingena,Jiang, Jun,Lan, Yunjun,Li, Juan,Li, Xinhua,Liu, Hongxin,Wan, Junlin,Xiao, Hong-Ping

, p. 2198 - 2202 (2019)

A phosphoric acid catalyzed atroposelective Friedl?nder reaction was developed in which acetylacetone and a variety of 2′-substituted 2-Aminobenzophenones were successfully employed to give optically active biaryl quinolines in good yields and with high enantioselectivities.

Hf(OTf)4-Catalyzed highly diastereoselective synthesis of 1,3-disubstituted tetralin derivatives via benzylic C(sp3)-H bond functionalization

Yoshida, Taira,Mori, Keiji

supporting information, p. 4319 - 4322 (2017/04/21)

We report a highly diastereoselective synthesis of 1,3-disubstituted tetralin derivatives via Lewis acid catalyzed benzylic C(sp3)-H bond functionalization. The employment of Hf(OTf)4 as an acid catalyst was crucial in the reaction,

Palladium(0)-catalyzed arylative dearomatization of phenols

Rousseaux, Sophie,Garcia-Fortanet, Jorge,Del Aguila Sanchez, Miguel Angel,Buchwald, Stephen L.

, p. 9282 - 9285 (2011/08/04)

The palladium-catalyzed arylative dearomatization of phenols to yield spirocyclohexadienone products in good to excellent yields has been developed. Preliminary results demonstrate that the formation of the spirocyclic all-carbon quaternary center can be accomplished with high levels of enantiocontrol (up to 91% ee).

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