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Structure of 898746-46-8
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1H-Pyrrolo[2,3-b]pyridine-6-carbaldehyde features a fused heterocyclic core with a reactive aldehyde handle at the 6-position, enabling direct incorporation into conjugation workflows. The electron-deficient pyrrolopyridine scaffold supports efficient coupling under mild conditions, offering enhanced stability and solubility in polar organic media. This compound serves as a valuable building block for bioactive molecule synthesis.
1H-Pyrrolo[2,3-b]pyridine-6-carbaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient access to bioactive scaffolds through standard carbonyl transformations. Its aldehyde functionality facilitates reductive amination, Wittig reactions, and nucleophilic addition, while the fused pyrrolopyridine core provides structural rigidity and enhanced π-conjugation. The compound exhibits good bench stability and is compatible with common protecting group strategies, making it well-suited for medicinal chemistry campaigns and process-scale applications.
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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: