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Structure of 1353101-49-1
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Methyl 1H-pyrrolo[3,2-c]pyridine-3-carboxylate features a fused heterocyclic core with a strategically positioned ester group, enabling direct incorporation into diverse synthetic sequences. The pyrrolopyridine scaffold imparts enhanced electron density and planarity, facilitating efficient coupling reactions. This bench-stable compound serves as a key intermediate in the development of bioactive molecules, particularly within kinase inhibitor and CNS-targeted drug discovery programs.
Methyl 1H-pyrrolo[3,2-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, while the ester group supports selective reduction or derivatization. Bench-stable and readily purified by chromatography, it functions as a key scaffold in the synthesis of kinase inhibitors and other 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: