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Structure of 867034-08-0
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7-Chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid features a rigid, electron-deficient heterocyclic core that integrates seamlessly into bioactive scaffolds. The carboxylic acid group enables direct coupling or derivatization under standard conditions, while the chloro substituent enhances electrophilic reactivity and modulates electronic properties for targeted molecular design in medicinal chemistry applications.
7-Chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to pyrrolopyridine-based scaffolds prevalent in medicinal chemistry. The carboxylic acid functionality facilitates direct coupling reactions, while the chloro substituent provides a handle for palladium-catalyzed cross-coupling transformations. Bench-stable and compatible with standard purification methods, it functions effectively in multistep syntheses requiring functional group tolerance and structural rigidity.
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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-H317
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Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: