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Structure of 84-59-3
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2,6-Dibromonaphthalene-1,5-diol features two bromine atoms at the 2 and 6 positions flanking a naphthalene core bearing hydroxyl groups at the 1 and 5 sites. This arrangement delivers enhanced electrophilic reactivity and stability under standard conditions, enabling direct incorporation into cross-coupling and functionalization workflows. The molecule’s electron-deficient aromatic system supports efficient metal-mediated transformations while maintaining bench-stable handling characteristics.
2,6-Dibromonaphthalene-1,5-diol serves as a versatile building block in the synthesis of functionalized naphthalene scaffolds, enabling selective coupling reactions via its bromine and phenolic functionalities. The molecule exhibits good bench stability and facilitates orthogonal transformations, allowing for sequential derivatization in complex molecule assembly. Its defined substitution pattern supports predictable reactivity in palladium-catalyzed cross-coupling and electrophilic functionalization, making it well-suited for applications in materials science and medicinal chemistry research.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H315-H318-H335
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Precautionary Statements : P280-P302+P352
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Lot numbers can be found on the outside label of a product: