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Structure of 496-69-5
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2-Bromo-4-fluorophenol features a phenolic hydroxyl group flanked by bromine and fluorine substituents, creating a uniquely reactive platform for cross-coupling and electrophilic functionalization. This electron-deficient aryl scaffold enables selective transformations under mild conditions, delivering high yields in Suzuki-Miyaura and Buchwald-Hartwig reactions. The molecule exhibits excellent stability during storage and handling, making it a reliable intermediate for pharmaceutical and agrochemical synthesis.
2-Bromo-4-fluorophenol serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient Suzuki-Miyaura and Stille couplings due to its well-defined halogen reactivity. The bromo group facilitates palladium-catalyzed cross-coupling, while the fluorine enhances metabolic stability and modulates electronic properties. Its bench-stable crystalline form simplifies handling and purification, making it ideal for multi-step synthetic sequences requiring functional group tolerance and predictable regiochemistry.
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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: