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2-AMINO-5-BENZYLTHIO-1,3,4-THIADIAZOLE CAS:25660-71-3

2-Amino-5-benzylthio-1,3,4-thiadiazole is an organic compound featuring a thiadiazole ring with amino and benzylthio substituents. This unique structure imparts significant reactivity and potential biological activity, making it a valuable target in medicinal chemistry and materials science. The presence of both amino and thiol groups allows for various chemical modifications, opening pathways for synthesizing novel derivatives with enhanced properties.

 


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Application and Effect:

2-Amino-5-benzylthio-1,3,4-thiadiazole has several important applications across different fields, primarily due to its distinctive chemical structure and potential biological activities. One of the key uses of this compound lies in pharmaceutical research, where it serves as a precursor or building block for synthesizing various bioactive molecules. The amino and benzylthio functional groups enable extensive chemical modifications that can enhance the pharmacological profiles of derivatives. Researchers are particularly interested in exploring its potential as an antimicrobial, antifungal, or anticancer agent, contributing to ongoing drug discovery efforts aimed at finding novel therapeutic agents. In addition to its pharmaceutical applications, 2-amino-5-benzylthio-1,3,4-thiadiazole is utilized in organic synthesis. Its diverse functional groups facilitate participation in various chemical reactions, such as electrophilic substitutions and cyclization processes. These reactions allow chemists to create more complex structures that could be relevant in the development of specialty chemicals, including dyes, agrochemicals, and other fine chemicals. Moreover, this compound has gained attention in the field of materials science due to its ability to form coordination complexes with metals. Such complexes can exhibit interesting electronic and optical properties, making them suitable for applications in sensors, catalysts, and photonic devices. The incorporation of 2-amino-5-benzylthio-1,3,4-thiadiazole into polymers or other material matrices may lead to improved performance characteristics for various applications. Additionally, the compound's potential applications in environmental chemistry are being explored. Its reactive thiol group may enable it to act as a chelating agent for heavy metal ions, which could contribute to remediation strategies in contaminated environments. By binding to pollutants, it may help mitigate their environmental impact. Lastly, ongoing investigations into the biological mechanisms and interactions associated with 2-amino-5-benzylthio-1,3,4-thiadiazole could yield critical insights into its efficacy and safety as a therapeutic agent. Understanding these interactions may inform the design of more effective drugs and improve the overall understanding of its applications in medicine. Overall, the versatility and potential of 2-amino-5-benzylthio-1,3,4-thiadiazole underscore its significance in scientific research and industrial applications, paving the way for future innovations and discoveries.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C9H9N3S2
Assay 99%
Appearance white powder
CAS No.  25660-71-3
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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