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Structure of 1192472-59-5
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tert-Butyl (5-ethynylpyridin-3-yl)carbamate features a pyridine ring bearing an ethynyl group at the 5-position and a tert-butyloxycarbonyl-protected amine at the 3-position. This bifunctional scaffold enables efficient coupling in copper-catalyzed click reactions and serves as a stable precursor for bioconjugation and medicinal chemistry applications, where the protected amine can be selectively deprotected under mild conditions.
tert-Butyl (5-ethynylpyridin-3-yl)carbamate serves as a versatile building block for the synthesis of pyridine-based scaffolds, enabling efficient Sonogashira coupling and copper-catalyzed azide–alkyne cycloaddition (CuAAC) reactions. The protected amine and terminal alkyne functionalities offer orthogonal reactivity, facilitating modular construction of complex heterocycles. Its bench-stable nature and ease of purification make it well-suited for iterative synthetic campaigns in medicinal chemistry and process development.
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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: