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[1,2,4]Triazolo[1,5-a]pyrimidine-2-sulfonamide, N-(2,6-dichlorophenyl)-5-methyl, is a complex organic compound with the molecular formula C10H7Cl2N5O2S. It features a triazolo[1,5-a]pyrimidine core, which is a fused-ring system consisting of a triazole and a pyrimidine. The compound is characterized by a sulfonamide group attached to the 2-position of the triazolo[1,5-a]pyrimidine ring and a 2,6-dichlorophenyl group at the nitrogen atom. Additionally, a methyl group is present at the 5-position of the triazolo[1,5-a]pyrimidine. [1,2,4]Triazolo[1,5-a]pyrimidine-2-sulfonamide, N-(2,6-dichlorophenyl)-5-methyl- is of interest in medicinal chemistry due to its potential as a pharmacophore in the development of new drugs, particularly in the area of antiviral and anticancer research. Its specific structure allows for interactions with biological targets, making it a candidate for further investigation in drug discovery processes.

98967-26-1

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98967-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98967-26-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,9,6 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 98967-26:
(7*9)+(6*8)+(5*9)+(4*6)+(3*7)+(2*2)+(1*6)=211
211 % 10 = 1
So 98967-26-1 is a valid CAS Registry Number.

98967-26-1Downstream Products

98967-26-1Relevant academic research and scientific papers

Process for the preparation of substituted N-(aryl)-1,2,4-triazolopyrimidine-2-sulfonamides

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, (2008/06/13)

The preparation of N-(aryl)-1,2,4-triazolopyrimidine-2-sulfonamides by the coupling of substituted 1,2,4-triazolopyrimidine-2-sulfonyl halides with aryl amines of substantially reduced nucleophilic reactivity is facilitated by conducting the reaction in t

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