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Structure of 849805-25-0
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Methyl 2-amino-6-chloropyridine-3-carboxylate features a fused pyridine core with complementary amino and chloro substituents, enabling selective functionalization in heterocyclic synthesis. The ester group provides enhanced solubility and reactivity under standard conditions, while the electron-donating amino moiety directs electrophilic substitution. This compound serves as a key intermediate for bioactive molecules in medicinal chemistry and agrochemical development.
Methyl 2-amino-6-chloropyridine-3-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyridine-based scaffolds through palladium-catalyzed cross-coupling and electrophilic substitution reactions. The ortho-amino and chloro groups provide complementary sites for sequential functionalization, while the ester moiety supports derivatization via hydrolysis or reduction. Its bench-stable nature and compatibility with standard reaction conditions facilitate reliable use in medicinal chemistry and process development 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: