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ethyl 4-hydroxy-5-oxo-2-phenyl-1-(p-tolyl)-2,5-dihydro-1H-pyrrole-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

147298-51-9

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147298-51-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147298-51-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,2,9 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 147298-51:
(8*1)+(7*4)+(6*7)+(5*2)+(4*9)+(3*8)+(2*5)+(1*1)=159
159 % 10 = 9
So 147298-51-9 is a valid CAS Registry Number.

147298-51-9Downstream Products

147298-51-9Relevant academic research and scientific papers

Visible light-promoted synthesis of pyrrolidinone derivatives via Rose Bengal as a photoredox catalyst and their photophysical studies

Dutta, Arup,Rohman, Mostofa A.,Nongrum, Ridaphun,Thongni, Aiborlang,Mitra, Sivaprasad,Nongkhlaw, Rishanlang

supporting information, p. 8136 - 8148 (2021/05/21)

Herein, we report an intramolecular radical cyclization reaction towards the synthesis of pyrrolidinone derivatives via metal-free photoredox catalysis under irradiation from blue LEDs. Some of the remarkable features of this protocol include synthetic ef

A Br?nsted acid-catalyzed multicomponent reaction for the synthesis of highly functionalized γ-lactam derivatives

Corte, Xabier del,de Marigorta, Edorta Martinez,Palacios, Francisco,Vicario, Javier

, (2019/08/22)

Br?nsted acids catalyze a multicomponent reaction of benzaldehyde with amines and diethyl acetylenedicarboxylate to afford highly functionalized γ-lactam derivatives. The reaction consists of a Mannich reaction of an enamine to an imine, both generated in situ, promoted by a phosphoric acid catalyst and a subsequent intramolecular cyclization. The hydrolysis of the cyclic enamine substrate can provide enol derivatives and, moreover, a second attack of the amine on the carboxylate can afford amide derivatives. An optimization of the reaction conditions is presented in order to obtain selectively cyclic enamines that can afford the enol species after selective hydrolysis.

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