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Structure of 1000341-64-9
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6-Chloro-1H-pyrrolo[3,2-c]pyridine-3-carbaldehyde features a rigid heteroaromatic core with a chlorinated pyrrolopyridine scaffold and a reactive aldehyde handle. This electron-deficient system enables direct coupling in cross-coupling reactions and facilitates incorporation into bioactive scaffolds. The aldehyde group offers site-specific functionalization under mild conditions, enhancing synthetic efficiency in medicinal chemistry workflows.
6-Chloro-1H-pyrrolo[3,2-c]pyridine-3-carbaldehyde serves as a versatile building block for the synthesis of heterocyclic scaffolds in medicinal chemistry. The aldehyde functionality enables direct incorporation into Ugi-type reactions and reductive amination workflows, while the chloro substituent supports palladium-catalyzed cross-coupling transformations. Bench-stable and compatible with standard protecting group strategies, it facilitates efficient access to complex pyrrolopyridine-based API candidates.
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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: