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2-(ethyl(phenyl)amino)-1-phenylethan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32119-56-5

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32119-56-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32119-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,1 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32119-56:
(7*3)+(6*2)+(5*1)+(4*1)+(3*9)+(2*5)+(1*6)=85
85 % 10 = 5
So 32119-56-5 is a valid CAS Registry Number.

32119-56-5Relevant academic research and scientific papers

A photoredox catalyzed radical-radical coupling reaction: Facile access to multi-substituted nitrogen heterocycles

Li, Weipeng,Duan, Yingqian,Zhang, Muliang,Cheng, Jian,Zhu, Chengjian

supporting information, p. 7596 - 7599 (2016/07/06)

Visible light induced photoredox catalysis is an efficient method for radical activation. Herein, we report the photoredox catalysis involving an intramolecular radical-radical coupling reaction that proceeds through a biradical intermediate. This protocol represents a new synthetic route to construct multi-substituted N-heterocycles. Four, five and six-membered N-heterocyclic structures with a quaternary carbon center are accessible under mild conditions.

N-Bromosuccinimide promoted and base switchable one pot synthesis of α-imido and α-amino ketones from styrenes

Shinde, Mahesh H.,Kshirsagar, Umesh A.

supporting information, p. 858 - 861 (2016/01/15)

An N-Bromosuccinimide (NBS) promoted one pot strategy for the synthesis of α-amino functionalized aryl ketones starting from commercially available styrenes has been developed. NBS participates in multiple tasks, such as bromonium ion formation, oxidation of bromohydrin and providing a nucleophilic nitrogen source. The reaction can easily be switched between α-imido and α-amino ketones by the choice of base. This one pot strategy was successfully applied for the synthesis of psychoactive drug candidates, amfepramone, mephedrone and 4-MEC.

Cyclisation indolique selon Bischler en presence d'acides de Lewis

Galons, Herve,Girardeau, Jean-Francois,Farnoux, Claude Combet,Miocque, Marcel

, p. 561 - 564 (2007/10/02)

In a comparative study of various catalysts (hydrochloric acid, Lewis acids) in the Bischler cyclization of α-aminoketones to indoles, aluminium chloride appears as the most active catalyst.Isomerization of β to α-indoles can be observed by raising the reaction temperature.The mechanism seems different from the one frequently suggested by most authors, since it does not affect intermediate aminoketones but indoles.

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