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Structure of 127094-57-9
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Ethyl 4,6-dichloro-1,5-naphthyridine-3-carboxylate features a sterically hindered naphthyridine core bearing two chlorine substituents at electron-deficient positions, enabling selective functionalization. The ester group facilitates downstream derivatization, while the molecule exhibits bench-stable handling under standard conditions. This compound serves as a key scaffold for synthesizing advanced heterocyclic systems in medicinal chemistry and materials science.
Ethyl 4,6-dichloro-1,5-naphthyridine-3-carboxylate serves as a versatile building block in medicinal chemistry, enabling selective functionalization at the 4- and 6-positions via palladium-catalyzed cross-coupling. The dichloro substitution pattern facilitates sequential derivatization, while the ester group supports further transformations. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for constructing complex naphthyridine-based scaffolds in API development.
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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: