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Structure of 10165-86-3
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Methyl 6-formylnicotinate features a formyl group at the C6 position of the nicotinate ring, enabling direct functionalization in synthetic sequences. This electron-deficient heterocycle integrates readily into cross-coupling and conjugation workflows, offering high reactivity under mild conditions. The ester moiety enhances solubility in organic solvents while maintaining stability during standard bench handling.
Methyl 6-formylnicotinate serves as a versatile building block in synthetic organic chemistry, enabling direct access to functionalized pyridine derivatives. The ortho-formyl group facilitates efficient aldol, Mannich, and reductive amination reactions, while the ester moiety supports selective transformations under mild conditions. Its bench-stable nature and compatibility with common protecting group strategies make it well-suited for multi-step synthesis of heterocyclic scaffolds and medicinal chemistry intermediates.
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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: