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Benzoic acid, 4-(3-methyl-5-phenyl-1H-pyrazol-1-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93323-55-8

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93323-55-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93323-55-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,3,2 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93323-55:
(7*9)+(6*3)+(5*3)+(4*2)+(3*3)+(2*5)+(1*5)=128
128 % 10 = 8
So 93323-55-8 is a valid CAS Registry Number.

93323-55-8Downstream Products

93323-55-8Relevant academic research and scientific papers

Polymer-supported quenching reagents for parallel purification

Booth, R. John,Hodges, John C.

, p. 4882 - 4886 (1997)

The preparation of polystyrene-divinylbenzene-supported derivatives of tris(2-aminoethyl)amine and methyl isocyanate are described. These polymeric reagents are used to quench excess reactants and remove known impurities from the crude reaction products o

Design, synthesis and anticandidal evaluation of indazole and pyrazole derivatives

Rodríguez-Villar, Karen,Hernández-Campos, Alicia,Yépez-Mulia, Lilián,Sainz-Espu?es, Teresita Del Rosario,Soria-Arteche, Olivia,Palacios-Espinosa, Juan Francisco,Cortés-Benítez, Francisco,Leyte-Lugo, Martha,Varela-Petrissans, Bárbara,Quintana-Salazar, Edgar A.,Pérez-Villanueva, Jaime

, p. 1 - 19 (2021/03/16)

Candidiasis, caused by yeasts of the genus Candida, is the second cause of superficial and mucosal infections and the fourth cause of bloodstream infections. Although some antifungal drugs to treat candidiasis are available, resistant strains to current therapies are emerging. Therefore, the search for new candicidal compounds is certainly a priority. In this regard, a series of indazole and pyrazole derivatives were designed in this work, employing bioisosteric replacement, homologa-tion, and molecular simplification as new anticandidal agents. Compounds were synthesized and evaluated against C. albicans, C. glabrata, and C. tropicalis strains. The series of 3-phenyl-1H-indazole moiety (10a–i) demonstrated to have the best broad anticandidal activity. Particularly, compound 10g, with N,N-diethylcarboxamide substituent, was the most active against C. albicans and both miconazole susceptible and resistant C. glabrata species. Therefore, the 3-phenyl-1H-indazole scaf-fold represents an opportunity for the development of new anticandidal agents with a new chemo-type.

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