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Structure of 869335-48-8
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1-Methyl-1H-pyrrolo[2,3-b]pyridin-4-amine features a fused heterocyclic core with a methylated pyrrole nitrogen and a primary amine at the C4 position. This scaffold delivers enhanced solubility and metabolic stability, enabling direct incorporation into kinase inhibitors and bioactive small molecules. The electron-rich aromatic system facilitates efficient coupling in transition-metal-catalyzed reactions under standard conditions.
1-Methyl-1H-pyrrolo[2,3-b]pyridin-4-amine serves as a versatile heterocyclic building block for medicinal chemistry and catalytic synthesis. Its electron-rich pyrrolopyridine core enables efficient palladium-catalyzed coupling reactions, while the N-methylated nitrogen enhances metabolic stability and modulates basicity. The amine functionality facilitates straightforward derivatization, including acylation and alkylation, supporting rapid library generation. Bench-stable and readily purified by standard chromatography, it functions as a key scaffold in the development of kinase inhibitors and other bioactive 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: