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Structure of 341-41-3
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1-Bromo-4-fluoronaphthalene features a strategically positioned bromine and fluorine substituent on the naphthalene core, enabling selective cross-coupling reactions. The electron-deficient aromatic system enhances reactivity in palladium-catalyzed transformations, while the orthogonal functional groups allow sequential derivatization. This bench-stable compound integrates readily into complex molecular architectures.
1-Bromo-4-fluoronaphthalene serves as a versatile building block in cross-coupling reactions, enabling efficient C–C bond formation via palladium-catalyzed methodologies. The orthogonal reactivity of bromo and fluoro substituents allows sequential functionalization, while the naphthalene core provides structural rigidity and π-conjugation suitable for pharmaceutical and materials applications. Bench-stable and readily purified, it functions reliably in standard synthetic 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: