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(S)-6-bromo-2-(2,4-dimethoxy-benzyl)-4-vinyl-3,4-dihydro-2H-pyrrolo[1,2-a]pyrazin-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

943587-56-2

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943587-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 943587-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,5,8 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 943587-56:
(8*9)+(7*4)+(6*3)+(5*5)+(4*8)+(3*7)+(2*5)+(1*6)=212
212 % 10 = 2
So 943587-56-2 is a valid CAS Registry Number.

943587-56-2Relevant academic research and scientific papers

Enantioselective Synthesis of Pyrrole-Fused Piperazine and Piperazinone Derivatives via Ir-Catalyzed Asymmetric Allylic Amination

Zhuo, Chun-Xiang,Zhang, Xiao,You, Shu-Li

, p. 5307 - 5310 (2016)

Ir-catalyzed intramolecular asymmetric allylic amination reaction of pyrrole derivatives was achieved. The pyrrole-fused piperazine and piperazinone derivatives could be easily accessed from the pyrrole-tethered allylic carbonates in good yields and enant

Asymmetric annulation toward pyrrolopip erazinones: Concise enantioselective syntheses of pyrrole alkaloid natural products

Trost, Barry M.,Dong, Guangbin

, p. 2357 - 2359 (2007)

A novel Pd-catalyzed asymmetric annulation between 5-bromopyrrole-2- carboxylate esters and vinyl aziridines has been developed to efficiently construct pyrrolopiperazinones, which can serve as key intermediates in the enantioselective syntheses of pyrrol

Palladium-catalyzed dynamic kinetic asymmetric transformations of vinyl aziridines with nitrogen heterocycles: Rapid access to biologically active pyrroles and indoles

Trost, Barry M.,Osipov, Maksim,Dong, Guangbin

supporting information; experimental part, p. 15800 - 15807 (2011/02/21)

We report that nitrogen heterocycles can serve as competent nucleophiles in the palladium-catalyzed dynamic kinetic asymmetric alkylation of vinyl aziridines. The resulting alkylated products were obtained with high regio-, chemo-, and enantioselectivity.

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