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Structure of 183803-12-5
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5-Bromo-2,4-dichlorophenol features a brominated aromatic ring with strategically positioned chloro substituents, delivering enhanced electrophilic reactivity. This electron-deficient scaffold integrates readily into cross-coupling and Ullmann-type transformations. The compound exhibits bench-stable handling under standard conditions, enabling reliable use in synthetic sequences requiring halogen-directed functionalization.
5-Bromo-2,4-dichlorophenol serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient functionalization via palladium-catalyzed cross-coupling reactions. Its bromine substituent provides high reactivity for Suzuki, Stille, and Negishi couplings, while the phenolic hydroxyl group offers orthogonal handling for protection or derivatization. The molecule exhibits excellent bench stability and facilitates purification by recrystallization, making it well-suited for scalable synthesis of complex heterocyclic scaffolds and API intermediates.
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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: