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Structure of 60666-70-8
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This bromochlorophenyl methanol features a reactive benzyl alcohol handle flanked by electron-withdrawing halogens, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. The ortho-bromo and meta-chloro substituents enhance regioselectivity while maintaining bench-stable handling under standard conditions.
(2-Bromo-5-chlorophenyl)methanol serves as a versatile aryl building block in medicinal chemistry and process development, enabling direct functionalization at the benzylic position. Its dual halogenation pattern provides orthogonal reactivity for cross-coupling reactions, 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 suitable for scale-up and multi-step synthesis workflows.
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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: