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1,3,4-Thiadiazole,2-(methylsulfonyl)-5-(trifluoromethyl)- CAS:27603-25-4

1,3,4-Thiadiazole, 2-(methylsulfonyl)-5-(trifluoromethyl)- is a heterocyclic compound featuring a thiadiazole ring system substituted with a methylsulfonyl group and a trifluoromethyl group. With the molecular formula C₅H₄F₃N₃O₂S, this compound has garnered attention in various fields, particularly in medicinal chemistry and agricultural chemistry. Its unique structural features contribute to its diverse biological activities, including antifungal and antibacterial properties. Ongoing research aims to explore its potential as a lead compound for developing novel pharmaceuticals and agrochemicals, leveraging its reactivity and ability to interact with biological targets.


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Application and Effect:

1,3,4-Thiadiazole, 2-(methylsulfonyl)-5-(trifluoromethyl)- is a member of the thiadiazole family, characterized by a five-membered ring containing two nitrogen atoms and three carbon atoms, with sulfur incorporated into its structure. The presence of the methylsulfonyl (-SO₂CH₃) and trifluoromethyl (-CF₃) substituents enhances the compound's stability and reactivity, making it an appealing candidate for various applications in drug discovery and agricultural chemistry. One of the key areas of interest for this compound is its potential biological activity. Research has demonstrated that derivatives of thiadiazoles often exhibit significant antimicrobial, antifungal, and antiviral properties. The methylsulfonyl group can enhance solubility and bioavailability, while the trifluoromethyl moiety contributes to increased lipophilicity, improving cell membrane penetration. As a result, 1,3,4-thiadiazole, 2-(methylsulfonyl)-5-(trifluoromethyl)- has been investigated for its possible utility in treating infections caused by resistant strains of bacteria and fungi. In addition to its pharmacological applications, this compound plays a role in agricultural chemistry. Thiadiazole derivatives have been explored for their ability to act as fungicides and herbicides. The incorporation of a methylsulfonyl group may enhance the selectivity and effectiveness of these compounds against specific plant pathogens. Furthermore, the unique electronic properties provided by the trifluoromethyl group can influence the compound's interaction with biological targets, paving the way for the development of selective inhibitors or modulators. Despite its promising potential, safety and toxicity evaluations are crucial when assessing the application of 1,3,4-thiadiazole, 2-(methylsulfonyl)-5-(trifluoromethyl)-. Comprehensive studies focusing on its pharmacokinetics, mechanism of action, and environmental impact will be necessary to ensure its viability as a therapeutic or agricultural agent. Overall, this compound represents a noteworthy avenue for exploration in both pharmaceutical and agrochemical research, contributing to the development of new tools for addressing modern health and agricultural challenges.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C4H3F3N2O2S2
Assay 99%
Appearance white powder
CAS No.  27603-25-4
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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