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Structure of 800401-65-4
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1H-Pyrrolo[3,2-c]pyridine-2-carboxylic acid features a fused heterocyclic core with a carboxylic acid group at the 2-position, enabling direct incorporation into bioactive scaffolds. The electron-deficient pyridine ring enhances reactivity in coupling reactions, while the acidic proton facilitates salt formation and solubility modulation. This structure serves as a key building block for pharmaceutical intermediates and functional materials.
1H-Pyrrolo[3,2-c]pyridine-2-carboxylic acid serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to structurally diverse scaffolds. Its carboxylic acid functionality facilitates direct amidation, esterification, and coupling reactions, while the fused pyrrolopyridine core exhibits favorable stability and compatibility with common reaction conditions. This compound functions as a key intermediate in the synthesis of kinase inhibitors and other bioactive molecules, offering robust reactivity and straightforward purification.
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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: