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Structure of 1341037-48-6
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This pyrrolopyridine derivative features a tert-butoxycarbonyl-protected amine and a carboxylic acid group, enabling direct incorporation into peptide coupling workflows. The electron-deficient heterocycle facilitates transition metal-catalyzed transformations, while the Boc moiety offers stability under standard bench conditions.
1-(tert-Butoxycarbonyl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid serves as a versatile building block for the synthesis of pyrrolopyridine-based scaffolds. The tert-butyl ester group provides excellent bench stability and facilitates purification, while the carboxylic acid enables straightforward derivatization via amide coupling or decarboxylation. Its compatibility with standard peptide coupling conditions and functional group tolerance makes it ideal for modular construction of biologically relevant heterocycles in medicinal chemistry campaigns.
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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: