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Structure of 24334-19-8
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Ethyl 1H-pyrrolo[2,3-c]pyridine-2-carboxylate features a fused heterocyclic core combining pyrrole and pyridine rings, offering enhanced electron-rich character and structural rigidity. This scaffold integrates readily into synthetic routes for bioactive compounds, particularly in medicinal chemistry applications where planar aromatic systems are advantageous. The ester functionality enables further derivatization under standard conditions.
Ethyl 1H-pyrrolo[2,3-c]pyridine-2-carboxylate serves as a versatile heterocyclic building block for the synthesis of biologically relevant scaffolds. The molecule features a fused pyrrolo[2,3-c]pyridine core with an ester-functionalized C2 position, enabling facile derivatization via hydrolysis, reduction, or coupling reactions. Its bench-stable nature and compatibility with standard synthetic protocols make it a practical reagent for medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.
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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: