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Structure of 1266119-48-5
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tert-Butyl N-(4-aminopyridin-2-yl)carbamate features a protected 4-aminopyridin-2-yl moiety enabling direct incorporation into heterocyclic scaffolds. The tert-butyl carbamate group offers stability under basic conditions while permitting facile deprotection to reveal the primary amine. This derivative serves as a key intermediate in the synthesis of bioactive pyridine-based compounds, particularly in medicinal chemistry applications requiring controlled amine functionality.
tert-Butyl N-(4-aminopyridin-2-yl)carbamate serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based scaffolds. The protected amine facilitates orthogonal functionalization, while the pyridinyl nitrogen supports metal-catalyzed coupling reactions. Its bench-stable nature and compatibility with standard deprotection protocols streamline synthesis of bioactive compounds and heterocyclic intermediates.
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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: