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Structure of 92616-49-4
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4-Bromo-1-naphthonitrile features a naphthalene core functionalized with a bromine atom at the 4-position and a nitrile group at the 1-position, enabling direct incorporation into cross-coupling reactions. The electron-deficient aromatic system enhances reactivity in palladium-catalyzed transformations, while the nitrile moiety serves as a handle for downstream derivatization. This compound exhibits excellent stability under standard bench conditions and is compatible with a range of synthetic methodologies.
4-Bromo-1-naphthonitrile serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized naphthalene scaffolds. The bromo and cyano groups provide orthogonal reactivity for palladium-catalyzed cross-coupling and nucleophilic transformations, respectively. Its bench-stable nature and compatibility with standard reaction conditions facilitate straightforward purification and integration into multi-step syntheses of heterocyclic compounds and advanced 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: