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Structure of 717106-69-9
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Methyl 2-(6-chloropyridin-3-yl)acetate features a chloropyridine moiety linked via a methylene bridge to an ester group, enabling direct functionalization at the acetyl position. This bench-stable compound serves as a key intermediate in synthesizing bioactive heterocycles, particularly in pharmaceuticals targeting kinase pathways. The electron-deficient pyridine ring enhances reactivity in nucleophilic substitution processes.
Methyl 2-(6-chloropyridin-3-yl)acetate serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-containing scaffolds via palladium-catalyzed cross-coupling reactions. The ester functionality facilitates downstream derivatization, while the 6-chloropyridin-3-yl group provides a reliable handle for C–H functionalization and heterocycle construction. Bench-stable and compatible with standard synthetic workflows, it supports scalable synthesis of bioactive molecules.
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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: