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Structure of 15936-10-4
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2-Chloro-1,8-naphthyridine features a chlorine-substituted naphthyridine core that imparts enhanced reactivity in cross-coupling processes. This electron-deficient heterocycle integrates readily into pharmaceutical scaffolds and serves as a key building block in the synthesis of bioactive molecules.
2-Chloro-1,8-naphthyridine serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions due to its well-established reactivity at the C2 position. The chlorine atom provides high functional group tolerance and bench stability, facilitating efficient incorporation into complex heterocyclic scaffolds. Its rigid bicyclic structure enhances π-conjugation and electron-deficient character, making it valuable for constructing advanced API intermediates and organic semiconductors.
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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: