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Structure of 1234217-58-3
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Methyl 2-(2-bromopyridin-4-yl)acetate features a brominated pyridine core linked to a methyl ester-functionalized acetic acid side chain. This structure enables direct incorporation into cross-coupling reactions, where the bromine serves as a reactive handle for palladium-catalyzed transformations. The molecule exhibits excellent stability under standard handling conditions and demonstrates favorable solubility in common organic solvents, facilitating use in synthetic workflows requiring precise functional group placement.
Methyl 2-(2-bromopyridin-4-yl)acetate serves as a versatile building block for constructing pyridine-based heterocycles and pharmaceutical intermediates. The bromine at the 2-position enables palladium-catalyzed cross-coupling reactions, while the ester group facilitates further functionalization. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for iterative synthesis in medicinal chemistry 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: