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Structure of 13373-11-0
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2-Chloro-5-phenyl-1,3,4-thiadiazole features a fused heterocyclic core with orthogonal electron-withdrawing chlorine and phenyl substituents, enhancing its utility in medicinal chemistry. The thiadiazole scaffold provides metabolic stability and facilitates π-stacking interactions in target binding. This compound serves as a key building block for bioactive molecules, particularly in the development of kinase inhibitors and antimicrobial agents.
2-Chloro-5-phenyl-1,3,4-thiadiazole serves as a versatile building block in heterocyclic synthesis, enabling efficient construction of bioactive scaffolds. Its chloro group facilitates nucleophilic substitution and transition-metal-catalyzed coupling reactions, while the phenyl substituent enhances structural rigidity and π-stacking potential. The molecule exhibits excellent bench stability and compatibility with standard purification protocols, making it well-suited for iterative synthetic campaigns in medicinal chemistry and materials science.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: