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Structure of 2172597-24-7
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This propiolic acid derivative features a tert-butoxycarbonyl-protected pyrrolidine moiety, enabling direct incorporation into peptide-based scaffolds. The alkyne functionality supports efficient copper-catalyzed cycloadditions, facilitating rapid conjugation in bioorthogonal labeling and chemical biology applications.
3-(1-(tert-Butoxycarbonyl)pyrrolidin-3-yl)propiolic acid serves as a versatile building block for synthesizing pyrrolidine-containing heterocycles and bioactive scaffolds. The propiolic acid functionality enables efficient Sonogashira coupling, cyclization, and conjugate addition reactions, while the Boc-protected amine ensures stability and ease of purification. This reagent facilitates straightforward access to complex molecular architectures under standard laboratory conditions.
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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: