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Structure of 13659-23-9
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2-Bromo-5-chlorophenol features a phenolic hydroxyl group flanked by bromo and chloro substituents at the 2- and 5-positions, respectively. This electron-deficient aromatic system enables direct functionalization in cross-coupling reactions. The molecule exhibits enhanced stability under standard conditions and serves as a key intermediate in the synthesis of bioactive compounds and specialty polymers.
2-Bromo-5-chlorophenol serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient functionalization via Suzuki-Miyaura and Stille coupling reactions. Its orthogonal halogenation pattern provides predictable reactivity for sequential transformations, while the phenolic hydroxyl group facilitates derivatization or protection. The compound exhibits good bench stability and is readily purified by recrystallization, making it well-suited for scalable synthetic workflows.
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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: