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Structure of 16492-75-4
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5-Bromobenzene-1,2,3-triol features a bromine substituent at the 5-position of a trihydroxybenzene scaffold, delivering enhanced electron-withdrawing character and improved solubility in polar solvents. This structural motif enables efficient coupling reactions and serves as a key intermediate in synthesizing bioactive molecules and functionalized aromatics under standard conditions.
5-Bromobenzene-1,2,3-triol serves as a versatile building block in synthetic organic chemistry, enabling regioselective functionalization via palladium-catalyzed cross-coupling reactions. The bromine substituent facilitates efficient C–C bond formation while the three adjacent hydroxyl groups provide sites for derivatization or protection, offering excellent functional group tolerance and bench stability. Its utility is well-established in the synthesis of complex heterocycles and bioactive scaffolds.
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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: