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Structure of 1260670-05-0
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3-Bromo-8-chloro-1,7-naphthyridine features a dual halogenated naphthyridine core with orthogonal reactivity at the 3-bromo and 8-chloro positions. This electron-deficient scaffold enables selective cross-coupling transformations under palladium catalysis, facilitating rapid access to functionalized heterocyclic architectures in medicinal chemistry and materials science applications.
3-Bromo-8-chloro-1,7-naphthyridine serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions due to its dual halogen functionality. The bromo group offers high reactivity in Suzuki, Stille, and Negishi couplings, while the chloro substituent provides orthogonal reactivity for sequential functionalization. Bench-stable and readily purified by column chromatography, it facilitates efficient synthesis of complex heterocyclic scaffolds and advanced API 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: