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Structure of 1018678-37-9
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Methyl 4-amino-2-chloropyridine-3-carboxylate features a pyridine core bearing amino, chloro, and ester functionalities, enabling direct integration into heterocyclic scaffolds. The electron-rich amino group facilitates nucleophilic coupling, while the ortho-chloro substituent supports palladium-catalyzed cross-coupling. This bench-stable intermediate streamlines synthesis of bioactive compounds in medicinal chemistry and agrochemical development.
Methyl 4-amino-2-chloropyridine-3-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based scaffolds. The ortho-chloro and amino groups facilitate sequential functionalization via palladium-catalyzed cross-coupling and electrophilic substitution, while the ester group supports selective reduction or derivatization. Bench-stable and compatible with standard purification methods, it functions reliably in multi-step syntheses of bioactive heterocycles.
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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: