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Structure of 800401-68-7
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5-Chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid features a fused heterocyclic core with a chlorine substituent at the 5-position and a carboxylic acid group at the 2-position. This configuration enables direct incorporation into bioactive scaffolds, particularly in kinase inhibitor design and medicinal chemistry campaigns requiring electron-deficient aromatic systems with enhanced metabolic stability.
5-Chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid serves as a versatile building block for heterocyclic scaffolds in medicinal chemistry. Its carboxylic acid functionality enables direct derivatization via amide coupling or esterification, while the chloro and pyrrolopyridine core offer defined reactivity for Suzuki-Miyaura and Buchwald-Hartwig couplings. Bench-stable and readily purified by recrystallization, it functions efficiently in standard synthetic workflows 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: