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Structure of 695-96-5
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2-Bromo-4-chlorophenol features a phenolic hydroxyl group flanked by bromo and chloro substituents at the 2- and 4-positions, respectively. This electron-deficient aromatic system enables direct functionalization in cross-coupling reactions and serves as a key intermediate in pharmaceutical and agrochemical synthesis. The compound exhibits enhanced stability under standard bench conditions.
2-Bromo-4-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 halogen reactivity facilitates sequential transformations, while the phenolic hydroxyl group supports derivatization and metal complexation. The compound exhibits good bench stability and is readily purified by recrystallization or column chromatography, making it well-suited for scalable synthetic workflows.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2020
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: