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Structure of 220000-87-3
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4-Chloro-N-methyl-2-pyridinecarboxamide features a chlorinated pyridine core with a methylated amide group, delivering enhanced metabolic stability and improved membrane permeability. This configuration supports efficient integration into bioactive scaffolds for medicinal chemistry applications, particularly in kinase inhibitor development and CNS-targeted drug discovery.
4-Chloro-N-methyl-2-pyridinecarboxamide serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based scaffolds. Its chloro group facilitates nucleophilic substitution and palladium-catalyzed coupling reactions, while the N-methyl amide provides stability and favorable solubility. This compound demonstrates excellent bench stability and functional group tolerance, making it well-suited for iterative synthesis and scale-up in API 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 : 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: