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Structure of 1092352-37-8
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tert-Butyl 7-bromo-1H-indazole-1-carboxylate features a brominated indazole core with a robust tert-butyl ester handle, enabling direct incorporation into cross-coupling reactions. The electron-deficient aromatic system facilitates palladium-catalyzed transformations, while the bench-stable protecting group simplifies purification and handling under standard conditions.
tert-Butyl 7-bromo-1H-indazole-1-carboxylate serves as a versatile building block for the synthesis of brominated indazole derivatives, enabling efficient late-stage functionalization in medicinal chemistry and agrochemical research. The tert-butyl ester group offers excellent bench stability and facile removal under mild acidic conditions, while the bromine substituent provides a reliable handle for palladium-catalyzed cross-coupling reactions, including Suzuki, Stille, and Negishi transformations. Its compatibility with diverse reaction conditions makes it ideal for constructing complex heterocyclic scaffolds in high-purity formats.
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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: