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Structure of 116230-30-9
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7-Bromonaphthalen-2-ol features a bromine substituent at the 7-position of naphthalene, flanked by a phenolic hydroxyl group at the 2-position. This arrangement imparts enhanced reactivity in palladium-catalyzed cross-coupling reactions while maintaining stability under standard conditions. The electron-deficient aromatic core facilitates efficient functionalization in synthetic pathways targeting advanced intermediates for pharmaceuticals and materials science.
7-Bromonaphthalen-2-ol serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-defined bromine functionality and ortho-hydroxyl group. The molecule exhibits bench stability and facilitates efficient functionalization in Suzuki, Stille, and Negishi couplings, making it valuable for constructing complex naphthyl-containing scaffolds. Its dual reactivity profile supports the synthesis of advanced heterocycles and functionalized aromatic systems relevant to pharmaceutical and materials research.
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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: