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Structure of 67058-74-6
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1H-Pyrrolo[2,3-c]pyridine-3-carboxylic acid features a fused heterocyclic core with a carboxylic acid at the 3-position, enabling direct conjugation in medicinal chemistry scaffolds. The electron-deficient pyrrolopyridine framework supports robust coupling reactions and enhances metabolic stability in bioactive molecules. This bench-stable reagent integrates efficiently into diverse synthetic pathways requiring rigid, planar aromatic systems.
1H-Pyrrolo[2,3-c]pyridine-3-carboxylic acid serves as a versatile heterocyclic building block in medicinal chemistry, enabling the construction of bioactive scaffolds through standard coupling and functionalization reactions. Its carboxylic acid functionality facilitates direct amide formation, esterification, and metal-mediated transformations, while the fused polycyclic core exhibits favorable bench stability and compatibility with diverse reaction conditions. This compound functions as a key structural motif in the synthesis of kinase inhibitors and other targeted therapeutics.
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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: