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(Z)-4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-4-pyrazolylamino)-3-penten-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108137-74-2

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108137-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108137-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,1,3 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108137-74:
(8*1)+(7*0)+(6*8)+(5*1)+(4*3)+(3*7)+(2*7)+(1*4)=112
112 % 10 = 2
So 108137-74-2 is a valid CAS Registry Number.

108137-74-2Downstream Products

108137-74-2Relevant academic research and scientific papers

Structural studies of 4-aminoantipyrine derivatives

Cunha, Silvio,Oliveira, Shana M.,Rodrigues Jr., Manoel T.,Bastos, Rodrigo M.,Ferrari, Jailton,De Oliveira, Cecília M.A.,Kato, Lucília,Napolitano, Hamilton B.,Vencato, Ivo,Lariucci, Carlito

, p. 32 - 39 (2005)

Reaction of 4-aminoantipyrine with acetylacetone, ethyl acetoacetate, benzoyl isothiocyanate, phenyl isothiocyanate, maleic anhydride and methoxymethylene Meldrum's acid afforded a series of new antipyrine derivatives. The antibacterial activity of the synthesized compounds against Micrococcus luteus ATCC 9341, Staphilococcus aureus ATCC 29737, and Escherichia coli ATCC 8739 was evaluated and the minimal inhibitory concentration determined. Modest activity was found only to the maleamic acid obtained from the reaction of 4-aminoantipyrine and maleic anhydride. 1H NMR investigation of this maleamic acid showed that it is slowly converted to the corresponding toxic maleimide. The structures of three derivatives were determined by X-ray diffraction analysis.

ETUDE COMPARATIVE DE LA REACTIVITE DE COMPOSES β-DICARBONYLES ET DES ANALOGUES ENAMINOCARBONYLES VIS-A-VIS D'AMINES HETEROCYCLIQUES

Maquestiau, A.,Eynde, J.-J. vanden

, p. 641 - 648 (2007/10/02)

Reactions between five β-dicarbonyl compounds (1-5) or their enaminocarbonyl analogues (6-10) and three heterocyclic amines (12-14) are studied.The two types of carbonyl derivatives give rise to the formation of the same final products.Kinetic data are es

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