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Structure of 1379324-66-9
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2-Chlorobenzo[d]thiazole-7-carboxylic acid integrates a chlorinated benzothiazole core with a carboxylic acid handle, enabling direct conjugation or derivatization in synthetic workflows. This scaffold delivers enhanced electronic modulation and metabolic stability for medicinal chemistry applications.
2-Chlorobenzo[d]thiazole-7-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to bioactive scaffolds through palladium-catalyzed coupling reactions. The carboxylic acid functionality facilitates direct derivatization or activation for amide bond formation, while the chloro substituent supports further functionalization via cross-coupling. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for medicinal chemistry and process development 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+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: