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Structure of 1190319-18-6
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1H-Pyrrolo[3,2-b]pyridine-7-carboxylic acid features a fused heterocyclic core with a carboxylic acid handle at the 7-position, enabling direct conjugation or derivatization. The electron-deficient pyrrolopyridine scaffold enhances reactivity in transition metal-catalyzed couplings and supports integration into bioactive molecules. This bench-stable, moisture-tolerant building block facilitates rapid access to functionalized scaffolds for medicinal chemistry and materials science applications.
1H-Pyrrolo[3,2-b]pyridine-7-carboxylic acid serves as a versatile building block for heterocyclic scaffolds in medicinal chemistry. Its carboxylic acid functionality enables direct amidation, esterification, and coupling reactions, facilitating the synthesis of target molecules for drug discovery. The fused bicyclic core exhibits favorable stability and solubility profiles, supporting efficient purification and scalability in synthetic workflows.
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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: