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Structure of 13316-09-1
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7-Chloro-5-methylthiazolo[5,4-d]pyrimidine features a fused thiazolopyrimidine core with strategic chlorine and methyl substituents enabling enhanced electron-withdrawing character and metabolic stability. This scaffold integrates readily into kinase inhibitor designs and serves as a key heterocyclic building block in medicinal chemistry campaigns targeting purine-binding sites.
7-Chloro-5-methylthiazolo[5,4-d]pyrimidine serves as a versatile heterocyclic building block for medicinal chemistry and agrochemical research. Its fused thiazolo[5,4-d]pyrimidine core provides enhanced metabolic stability and facilitates diverse functionalization at the 7-chloro and 5-methyl positions. The molecule exhibits bench stability, good solubility in common organic solvents, and compatibility with standard cross-coupling and nucleophilic substitution protocols, enabling efficient access to complex scaffolds in drug discovery workflows.
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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-P305+P351+P338-P330-P362-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: