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Structure of 1234616-02-4
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1-Chloro-4-iodo-2,7-naphthyridine features a dual halogenated naphthyridine core with orthogonal reactivity, enabling selective cross-coupling transformations. The chlorine and iodine substituents facilitate sequential functionalization under palladium catalysis, while the electron-deficient ring system enhances stability and regioselectivity in C–C bond formation. This scaffold serves as a robust building block for advanced heterocyclic architectures.
1-Chloro-4-iodo-2,7-naphthyridine serves as a versatile bifunctional building block for transition-metal-catalyzed cross-coupling reactions. The chloro group enables palladium-catalyzed coupling with boronic acids or nucleophiles, while the iodo substituent offers high reactivity in Suzuki, Stille, and Negishi transformations. Its orthogonality allows sequential functionalization, and the naphthyridine core provides inherent stability and compatibility with diverse reaction conditions, making it ideal for constructing complex heterocyclic scaffolds in medicinal chemistry and materials science applications.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: