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Structure of 108128-12-7
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Methyl 1H-pyrrolo[2,3-c]pyridine-3-carboxylate features a fused heterocyclic core with a strategically positioned ester group enabling direct functionalization. This electron-deficient scaffold integrates readily into synthetic sequences requiring nitrogen-rich frameworks. The methyl ester facilitates downstream transformations without prior activation. The compound exhibits robust stability under standard bench conditions and demonstrates compatibility with diverse reaction environments.
Methyl 1H-pyrrolo[2,3-c]pyridine-3-carboxylate serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its pyrrolopyridine core enables efficient functionalization at the C3 position via palladium-catalyzed cross-coupling reactions. The ester group facilitates further derivatization, while the scaffold exhibits good bench stability and compatibility with standard synthetic protocols.
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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: