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1H-Pyrrole-2-carboxylic acid, 5-(2-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

403502-14-7

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403502-14-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 403502-14-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,3,5,0 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 403502-14:
(8*4)+(7*0)+(6*3)+(5*5)+(4*0)+(3*2)+(2*1)+(1*4)=87
87 % 10 = 7
So 403502-14-7 is a valid CAS Registry Number.

403502-14-7Relevant academic research and scientific papers

Phenylpyrrole derivatives as neural and inducible nitric oxide synthase (nNOS and iNOS) inhibitors

Lopez Cara, Luisa C.,Camacho, M. Encarnacion,Carrion, M. Dora,Tapias, Victor,Gallo, Miguel A.,Escames, Germaine,Acuna-Castroviejo, Dario,Espinosa, Antonio,Entrena, Antonio

experimental part, p. 2655 - 2666 (2009/10/09)

We have previously described a series of 3-phenyl-4,5-dihydro-1H-pyrazole derivatives as moderately potent nNOS inhibitors. As a follow up of these studies, several new 5-phenyl-1H-pyrrole-2-carboxamide derivatives have been synthesized, and their biologi

NMR and conformational studies of new 5-phenylpyrrole-carboxamide derivatives

Luisa, C. Lopez-Cara,De Las Infantas, M. Jose Pineda,Carrion, M. Dora,Camacho, M. Encarnacion,Gallo, Miguel A.,Espinosa, Antonio,Entrena, Antonio

scheme or table, p. 1101 - 1109 (2010/08/05)

The 1H and 13C NMR resonances of 22 5-(5-substituted-2-nitrophenyl)-1H-pyrrole-2-carboxamides, 22 5-(5-substituted-2-aminophenyl)-1H-pyrrole-2-carboxamides, and 9 5-phenyl-1H-pyrrole-2-carboxamides we

Synthesis and anti-HIV-1 activity of new delavirdine analogues carrying arylpyrrole moieties

Pinna,Loriga,Murineddu,Grella,Mura,Vargiu,Murgioni,La Colla

, p. 1406 - 1411 (2007/10/03)

In our search for novel anti-human immunodeficiency virus (HIV)-1 agents, 14 delavirdine analogues were synthesized and evaluated as potential anti-HIV-1 agents in cell-based assays. Compound 1Aa exhibited potent and selective anti-HIV-1 activity in acutely infected MT4 cells, with effective concentration (EC50) values in the submicromolar range.

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