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Structure of 917562-09-5
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This bromochlorophenylmethanol features a strategically positioned bromine and chlorine substituent on the aromatic ring, enabling selective functionalization in cross-coupling reactions. The primary alcohol group provides a direct handle for derivatization, while the electron-withdrawing halogens enhance reactivity in palladium-catalyzed processes. Bench-stable under standard conditions, it serves as a reliable building block for advanced synthetic intermediates.
(3-Bromo-5-chlorophenyl)methanol serves as a versatile building block in medicinal chemistry and materials synthesis, enabling direct functionalization at the benzylic position. Its dual halogenation pattern provides orthogonal reactivity for cross-coupling processes, while the primary alcohol facilitates derivatization via esterification, ether formation, or oxidation to aldehyde. The compound exhibits good bench stability and is compatible with standard purification techniques, making it well-suited for iterative synthetic sequences in API development and heterocycle construction.
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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: