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Structure of 877264-77-2
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tert-Butyl 6-bromo-1H-indazole-1-carboxylate features a brominated indazole core with a robust tert-butyl ester handle, enabling straightforward deprotection and functionalization. This bench-stable reagent integrates seamlessly into cross-coupling workflows, delivering access to diverse indazole-based scaffolds for medicinal chemistry and materials science applications.
tert-Butyl 6-bromo-1H-indazole-1-carboxylate serves as a versatile building block for the synthesis of brominated indazole derivatives, enabling direct functionalization via palladium-catalyzed cross-coupling reactions. The tert-butyl ester group offers excellent bench stability and facilitates straightforward deprotection under mild acidic conditions. Its compatibility with diverse reaction partners makes it ideal for constructing complex heterocyclic scaffolds in 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: