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Structure of 1018950-15-6
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tert-Butyl 1H-pyrrolo[3,2-b]pyridine-1-carboxylate features a robust pyrrolopyridine scaffold with a bench-stable tert-butyl ester handle, enabling straightforward deprotection and integration into complex heterocyclic architectures. This protected core facilitates efficient access to biologically active pyrrolo[3,2-b]pyridine derivatives under standard conditions.
tert-Butyl 1H-pyrrolo[3,2-b]pyridine-1-carboxylate serves as a versatile scaffold for constructing biologically relevant heterocycles, enabling efficient functionalization at the pyrrole nitrogen and pyridine ring positions. The tert-butyl carbamate group offers excellent bench stability and facilitates straightforward deprotection under mild acidic conditions, simplifying downstream synthesis. Its compatibility with palladium-catalyzed cross-coupling reactions and tolerance to diverse functional groups make it a practical building block in medicinal chemistry and process development 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: