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Structure of 877041-47-9
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6-O-tert-Butyl 3-O-methyl 2-amino-5,7-dihydro-4H-thieno[2,3-c]pyridine-3,6-dicarboxylate features a sterically shielded tert-butyl ether and methyl ester at the 6- and 3-positions, respectively, enhancing stability and solubility. The electron-rich thienopyridine core bears a strategically positioned amino group, enabling direct incorporation into diverse heterocyclic scaffolds via cross-coupling or cyclization reactions under standard conditions.
6-O-tert-Butyl 3-O-methyl 2-amino-5,7-dihydro-4H-thieno[2,3-c]pyridine-3,6-dicarboxylate serves as a versatile building block for the synthesis of thienopyridine-based heterocycles. The protected diester functionality enables selective transformations, while the 2-amino group facilitates downstream coupling and cyclization reactions. Bench-stable and compatible with standard synthetic protocols, it functions as a key intermediate in the construction of bioactive scaffolds relevant to medicinal chemistry and process development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: