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Structure of 3827-49-4
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2-Chloro-5-fluorophenol features a fluorinated aromatic ring with orthogonal halogen substituents, enabling selective coupling reactions in pharmaceutical synthesis. The electron-withdrawing chlorine and fluorine atoms enhance reactivity at the phenolic hydroxyl site while maintaining stability under standard conditions. This compound serves as a key intermediate in agrochemical and medicinal chemistry applications.
2-Chloro-5-fluorophenol serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the phenolic position while maintaining orthogonality with common protecting groups. Its halogenated aromatic core facilitates palladium-catalyzed cross-coupling reactions, and the hydroxyl group allows for derivatization via etherification or esterification. Bench-stable and readily purified by recrystallization, it supports scalable synthesis of fluorinated heterocycles 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: