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Structure of 1203498-99-0
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5-Chloro-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid features a fused heterocyclic core with a chlorine substituent at the 5-position and a carboxylic acid group at the 3-position. This electron-deficient scaffold integrates readily into medicinal chemistry campaigns, offering enhanced metabolic stability and favorable binding interactions in target-directed synthesis.
5-Chloro-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid serves as a versatile building block for the synthesis of bioactive heterocycles, particularly in medicinal chemistry and agrochemical research. Its structure features a chlorinated pyrrolopyridine core with a carboxylic acid functional group, enabling direct coupling reactions and derivatization via amide formation or esterification. The molecule exhibits good bench stability and facilitates efficient incorporation into complex scaffolds due to its well-defined reactivity and compatibility with standard synthetic protocols.
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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: