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Structure of 119285-07-3
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tert-Butyl 4-(5-aminopyridin-2-yl)piperazine-1-carboxylate features a pyridine nitrogen strategically positioned to enable direct functionalization, paired with a bench-stable tert-butyl carbamate protecting group. This combination facilitates efficient coupling reactions and simplifies purification in synthetic sequences targeting bioactive heterocycles.
tert-Butyl 4-(5-aminopyridin-2-yl)piperazine-1-carboxylate serves as a versatile building block for the synthesis of bioactive heterocycles, enabling direct access to pyridine-piperazine scaffolds common in medicinal chemistry. The tert-butyl carbamate group provides excellent bench stability and facilitates straightforward deprotection under mild acidic conditions. Its compatibility with standard coupling reactions and tolerance to diverse functional groups supports efficient integration into multi-step synthetic sequences.
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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: