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

31407-15-5

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31407-15-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31407-15-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,4,0 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 31407-15:
(7*3)+(6*1)+(5*4)+(4*0)+(3*7)+(2*1)+(1*5)=75
75 % 10 = 5
So 31407-15-5 is a valid CAS Registry Number.

31407-15-5Relevant academic research and scientific papers

A robust synthesis and characterization of superparamagnetic CoFe2O4 nanoparticles as an efficient and reusable catalyst for green synthesis of some heterocyclic rings

Aleem Ali El-Remaily, Mahmoud Abd El,Abu-Dief, Ahmed M.,El-Khatib, Rafat M.

, p. 1022 - 1029 (2016)

A robust synthesis for magnetic CoFe2O4 nanoparticles via a hydrothermal technique was investigated. The prepared magnetic nanoparticles were characterized using powder X-ray diffraction, scanning, transmission and high-resolution tr

Method for catalytic synthesis of 3-pyrroline-2-one in emulsion by synergizing titanocene dichloride with Bronsted acid

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Paragraph 0016; 0017; 0018; 0019; 0056; 0057; 0058-0060, (2019/02/04)

The invention discloses a method for catalytic synthesis of 3-pyrroline-2-one in the emulsion by synergizing titanocene dichloride with Bronsted acid. According to the method, a emulsion system is constructed by taking the titanocene dichloride and Bronst

Synthesis and Reaction with Oxalyl Chloride of Ethyl 1-Aryl-4,5-dioxo-2-pyrrolidinecarboxylates and Their 3-Arylamino Derivatives

Gein,Shumilovskikh,Voronina,Gein,Khokhryakova,Tendryakova,Vyaznikova,Andreichikov

, p. 1267 - 1270 (2007/10/03)

Ethyl piruvate was reacted with aromatic amines to obtain ethyl 1-aryl-4-arylamino-2-methyl-5-oxo-2,5-dihydropyrrol-1H-2-pyrrolecarboxylates. Hydrolysis of the latter with hydrochloric acid gave ethyl 1-aryl-2-methyl-4,5-dioxo-2-pyrrolidinecarboxylates. Oxalyl chloride reacts with the 4-arylamino derivatives to give ethyl 1,5-diaryl-4-methyl-2,3,6-dioxo-1,2,3,4,5,6-hexahydropyrrolo[3,4-b]pyrrole-4- carboxylates, and the reaction with 1-aryl-2-methyl-4,5-dioxo-2-pyrrolidinecarboxylates yields 1-aryl-1-(ethoxycarbonyl)-5-methyl-2-oxo-2,5-dihydro-1H-3-pyrrolyl) oxalates.

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