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2-phenyl-4-((2-phenylhydrazono)methyl)-2H-1,2,3-triazole is a complex organic compound characterized by its unique molecular structure. It is a derivative of 1,2,3-triazole, a heterocyclic compound with a five-membered ring containing three nitrogen atoms. The molecule features a phenyl group (C6H5) attached to the 2nd carbon of the triazole ring, and a phenylhydrazonomethyl group (C6H5-NH-NH-CH2) connected to the 4th carbon. 2-phenyl-4-((2-phenylhydrazono)methyl)-2H-1,2,3-triazole is of interest in chemical research due to its potential applications in various fields, such as pharmaceuticals and materials science, where its specific properties and reactivity can be harnessed. The compound's structure and properties make it a subject of study for chemists exploring the synthesis and applications of heterocyclic compounds.

6254-74-6

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6254-74-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6254-74-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,5 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6254-74:
(6*6)+(5*2)+(4*5)+(3*4)+(2*7)+(1*4)=96
96 % 10 = 6
So 6254-74-6 is a valid CAS Registry Number.

6254-74-6Relevant academic research and scientific papers

1-Phenyl-1H- and 2-phenyl-2H-1,2,3-triazol derivatives: Design, synthesis and inhibitory effect on alpha-glycosidases

Gonzaga, Daniel,Senger, Mario Roberto,Da Silva, Fernando De Carvalho,Ferreira, Vitor Francisco,Silva Jr., Floriano Paes

, p. 461 - 476 (2014/02/14)

Due to aging and increasingly overweight in human population, the incidence of non-insulin dependent diabetes mellitus (NIDDM or Type 2 DM) is increasing considerably. Therefore, searching for new α-glycosidase inhibitors (GIs) capable of slowing down carbohydrate assimilation by humans is an important strategy towards control of NIDDM. In this report, we disclose the search for new easily accessible synthetic triazoles as anti-diabetic compounds. Two series of non-glycosid triazoles were synthesized (series A and B) and screened against baker's yeast α-glucosidase (MAL12) and porcine pancreatic α-amylase activity (PPA). Of the 60 compounds tested at 500 μM, were considered hits (≥60% inhibition) six triazoles against MAL12 and three against PPA, with the inhibition reaching up to 99.4% on MAL12 and 88.6% on PPA. The IC50 values were calculated for both enzymes and ranged from 54 to 482 μM for MAL12 and 145 to 282 μM for PPA. These results demonstrated the potential activity of simple and non-glycosidic triazoles as an important novel class of GIs for the development of drugs to treat Type 2 DM.

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