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Structure of 885521-92-6
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6-Bromo-1H-indazol-3-ol features a brominated indazolol scaffold with a phenolic hydroxyl group, offering enhanced reactivity for cross-coupling and functionalization. The electron-deficient heterocycle facilitates transition-metal catalyzed transformations, while the hydroxyl moiety enables hydrogen bonding and strategic derivatization. This bench-stable compound serves as a key intermediate in medicinal chemistry and materials synthesis.
6-Bromo-1H-indazol-3-ol serves as a versatile building block for the synthesis of biologically active heterocycles, leveraging its bromine and phenolic hydroxyl groups for subsequent cross-coupling and functionalization. The molecule exhibits good bench stability and facilitates efficient derivatization via Pd-catalyzed reactions, enabling rapid access to substituted indazoles relevant in medicinal chemistry.
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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: