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Structure of 59488-60-7
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This thienopyridine carboxylic acid features a strategically positioned amino group and methyl substituent, enabling integration into bioactive scaffolds. The electron-rich heterocyclic core enhances π-stacking interactions, while the carboxylic acid facilitates conjugation or salt formation under standard conditions.
3-Amino-6-methylthieno[2,3-b]pyridine-2-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its fused thienopyridine core provides enhanced planarity and electronic delocalization, while the amino and carboxylic acid groups enable direct functionalization via amide coupling, acylation, or cyclization. The methyl group at the 6-position enhances metabolic stability and modulates lipophilicity. Bench-stable and readily purified by recrystallization, it functions effectively in standard peptide coupling and Suzuki-Miyaura cross-coupling protocols, facilitating efficient access to diverse analogs.
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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 : H317-H319
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Precautionary Statements : P261-P264-P272-P280-P302+P352-P362+P364-P501
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Lot numbers can be found on the outside label of a product: