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Structure of 16726-66-2
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3-Bromo-1-naphthoic acid features a bromine substituent at the 3-position of the naphthalene core, enhancing electrophilic reactivity and enabling direct functionalization in cross-coupling processes. The carboxylic acid group provides a handle for derivatization via esterification, amidation, or salt formation. This bench-stable compound serves as a key intermediate in the synthesis of bioactive naphthyl derivatives and functional materials.
3-Bromo-1-naphthoic acid serves as a versatile building block in synthetic organic chemistry, enabling direct functionalization at the naphthalene ring and facilitating subsequent cross-coupling reactions. Its bromine substituent provides high reactivity in palladium-catalyzed transformations, while the carboxylic acid group offers orthogonal functionality for derivatization. The compound exhibits excellent bench stability and is readily purified by recrystallization, making it ideal for iterative synthesis of complex heterocycles and pharmaceutical intermediates.
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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: