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Structure of 417721-36-9
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4-Chloro-7-methoxyquinoline-6-carboxamide features a quinoline core with strategically positioned electron-withdrawing and donor groups, enabling robust conjugation in synthetic transformations. The chloro and methoxy substituents enhance reactivity and solubility, while the carboxamide moiety provides a versatile handle for derivatization. This compound serves as a key scaffold in medicinal chemistry and materials science applications.
4-Chloro-7-methoxyquinoline-6-carboxamide serves as a versatile building block in medicinal chemistry, enabling efficient access to quinoline-based scaffolds through palladium-catalyzed cross-coupling reactions. Its chloro group facilitates C–C and C–N bond formation under standard conditions, while the methoxy and carboxamide functionalities offer orthogonal reactivity and enhanced solubility. The compound exhibits excellent bench stability and ease of purification, making it well-suited for high-throughput synthesis 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 : 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: