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Structure of 1009735-23-2
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Methyl 2-bromo-6-methoxynicotinate is a bench-stable, moisture-tolerant heterocyclic building block featuring a bromine at the C2 position and a methoxy group at C6. This regioselective substitution pattern enables efficient palladium-catalyzed coupling reactions, facilitating rapid access to functionalized pyridine derivatives in medicinal chemistry and materials synthesis.
Methyl 2-bromo-6-methoxynicotinate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined bromine handle. The methyl ester and methoxy groups provide orthogonal functionality for selective transformations, while the compound exhibits excellent bench stability and ease of purification—key attributes for scalable medicinal chemistry 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: