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Structure of 883107-62-8
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Methyl 3-amino-2,6-dichloroisonicotinate features a pyridine core with strategic chlorine substitutions and a terminal amino group, enabling direct incorporation into bioactive heterocycles. This bench-stable derivative facilitates rapid diversification in medicinal chemistry campaigns, particularly for kinase inhibitors and antimicrobial agents, due to its compatibility with cross-coupling and nucleophilic substitution reactions under standard conditions.
Methyl 3-amino-2,6-dichloroisonicotinate serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted pyridine scaffolds via standard coupling and cyclization protocols. The molecule exhibits bench stability, tolerates diverse functional groups, and facilitates efficient derivatization through its amino and ester functionalities, making it well-suited for parallel synthesis campaigns and API intermediate 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: