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Structure of 5428-40-0
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4-Bromo-2-hydroxybenzamide features a bromine atom at the para position relative to the amide group, combined with a phenolic hydroxyl for enhanced reactivity. This electron-deficient aromatic scaffold enables efficient coupling in cross-coupling and peptide synthesis workflows. The molecule exhibits excellent stability under standard bench conditions and facilitates direct functionalization of complex heterocycles.
4-Bromo-2-hydroxybenzamide serves as a versatile building block in medicinal chemistry, enabling direct incorporation into heterocyclic scaffolds via Ullmann-type couplings or electrophilic substitution. The ortho-hydroxyl group facilitates in situ activation for palladium-catalyzed cross-coupling, while the bromide supports reliable Suzuki and Stille reactions. Bench-stable and readily purified by recrystallization, it functions effectively in multi-step syntheses requiring orthogonal reactivity and functional group compatibility.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: