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Structure of 1190311-14-8
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Methyl 2-oxo-2,3-dihydro-1H-pyrrolo[3,2-b]pyridine-5-carboxylate features a fused bicyclic core with a carbonyl at the 2-position and an ester handle at C5, enabling direct functionalization. This bench-stable heterocycle integrates readily into synthetic sequences requiring electron-deficient pyrrolopyridine scaffolds for medicinal chemistry applications.
Methyl 2-oxo-2,3-dihydro-1H-pyrrolo[3,2-b]pyridine-5-carboxylate serves as a versatile heterocyclic building block for medicinal chemistry and synthetic organic applications. Its pyrrolo[3,2-b]pyridine core enables efficient functionalization at C5 via nucleophilic substitution or metal-catalyzed coupling. The methyl ester group facilitates downstream derivatization, while the ketone functionality supports enolate formation and conjugate addition reactions. Bench-stable and readily purified by column chromatography, it functions effectively in standard synthetic workflows requiring orthogonally reactive handles.
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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: