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Structure of 1067193-34-3
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5-Fluoro-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid features a fluorinated heterocyclic core with a carboxylic acid group at the 3-position, enabling direct conjugation or derivatization in medicinal chemistry. The electron-deficient pyrrolopyridine scaffold supports targeted interactions in kinase inhibition and protein binding studies. This bench-stable compound integrates readily into bioactive molecule design.
5-Fluoro-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid serves as a versatile building block for medicinal chemistry and heterocyclic synthesis, offering a well-defined scaffold with orthogonal functional handles. Its carboxylic acid group enables direct amidation, esterification, or coupling reactions, while the fluorinated pyrrolopyridine core provides enhanced metabolic stability and tunable electronic properties. The compound exhibits good bench stability and facilitates efficient purification, making it suitable for scalable synthesis of bioactive molecules and API intermediates.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: