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Structure of 1940-44-9
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4-Bromo-2,3-dichlorophenol features a brominated aromatic core with two chlorine substituents at ortho and meta positions relative to the phenolic hydroxyl. This electron-deficient scaffold enables direct coupling in cross-coupling reactions and serves as a key intermediate in pharmaceutical synthesis. The compound exhibits enhanced stability under standard bench conditions and integrates readily into complex molecular architectures.
4-Bromo-2,3-dichlorophenol serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient functionalization at the aromatic ring. Its ortho-chlorine substituents enhance regioselectivity in subsequent coupling reactions, while the phenolic hydroxyl group provides a handle for derivatization or metal coordination. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for use in Suzuki-Miyaura, Stille, and Ullmann-type transformations.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: