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Structure of 344327-11-3
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1H-Pyrrolo[2,3-b]pyridine-4-carbonitrile integrates a nitrogen-rich heterocyclic core with a terminal nitrile group, enabling direct functionalization in transition-metal-catalyzed cross-coupling reactions. This bench-stable scaffold features enhanced electron deficiency at the pyrrolopyridine ring, facilitating efficient incorporation into bioactive molecules and advanced materials.
1H-Pyrrolo[2,3-b]pyridine-4-carbonitrile serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to fused pyrrolopyridine scaffolds. Its nitrile group facilitates downstream functionalization via hydrolysis, reduction, or nucleophilic addition, while the electron-deficient core supports transition-metal-catalyzed coupling reactions. The compound exhibits good bench stability and is compatible with standard purification methods, making it suitable for iterative synthesis campaigns targeting 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: