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5-Amino-1,3,4-thiadiazole-2-thiol CAS:2349-67-9

5-Amino-1,3,4-thiadiazole-2-thiol is a heterocyclic compound characterized by the presence of both amino and thiol functional groups within a thiadiazole ring. With the molecular formula C₂H₃N₄S₂, this compound exhibits diverse biological activities, making it of significant interest in medicinal chemistry and agricultural applications. Its unique structure enables it to act as a potential lead compound for developing novel pharmaceuticals, particularly those aimed at treating infections or cancers. Ongoing research into its reactivity, stability, and biological interactions continues to reveal its potential as a valuable building block in synthetic organic chemistry.


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Application and Effect:

5-Amino-1,3,4-thiadiazole-2-thiol is a derivative of thiadiazole that contains an amino group (-NH₂) and a thiol group (-SH) positioned on the 1,3,4-thiadiazole ring system. The molecular formula of this compound is C₂H₃N₄S₂, and it has garnered attention in various fields, including pharmaceuticals and agrochemicals, due to its diverse chemical and biological properties. One of the primary areas of interest surrounding 5-amino-1,3,4-thiadiazole-2-thiol is its potential as an antimicrobial and antifungal agent. Preliminary studies suggest that compounds within the thiadiazole family exhibit notable activity against various pathogens, which makes them promising candidates for developing new therapeutic agents. The presence of the thiol group can enhance its reactivity, allowing it to participate in redox reactions and interact effectively with biological macromolecules, such as proteins and nucleic acids. In addition to its antimicrobial properties, 5-amino-1,3,4-thiadiazole-2-thiol may play a role in cancer therapy. Research has indicated that certain thiadiazole derivatives possess antitumor activity, potentially through mechanisms involving apoptosis induction and inhibition of cellular proliferation. This characteristic highlights the compound's potential as a scaffold for designing new anticancer drugs. Moreover, the compound's ability to form various derivatives by modifying the thiol or amino groups further expands its applications. These derivatives can be engineered to enhance efficacy, selectivity, and bioavailability, making them suitable for more specific therapeutic targets. However, while exploring these promising applications, safety assessments are essential. As with many sulfur-containing compounds, there may be concerns regarding toxicity or adverse effects during synthesis or application. Comprehensive studies focusing on pharmacokinetics, mechanisms of action, and environmental impact will contribute to the safe development of 5-amino-1,3,4-thiadiazole-2-thiol-based compounds in clinical and industrial contexts. In summary, 5-amino-1,3,4-thiadiazole-2-thiol represents an intriguing compound with considerable potential in medicinal chemistry and agriculture, warranting further investigation to unlock its full therapeutic and practical capabilities.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C2H3N3S2
Assay 99%
Appearance white powder
CAS No.  2349-67-9
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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