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Structure of 118080-82-3
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tert-Butyl N-[(2R)-but-3-yn-2-yl]carbamate features a chiral propargylic alcohol moiety flanked by a sterically hindered tert-butyl carbamate group, enabling selective protection in asymmetric synthesis. The alkyne handle facilitates efficient coupling reactions under mild conditions, while the bench-stable carbamate remains intact through standard organic transformations.
tert-Butyl N-[(2R)-but-3-yn-2-yl]carbamate serves as a versatile chiral building block for the synthesis of functionalized amino alcohols and nitrogen-containing heterocycles. Its propargylic carbamate functionality enables reliable copper-catalyzed azide-alkyne cycloaddition (CuAAC), while the tert-butyl carbamate group offers excellent stability and ease of removal under mild acidic conditions. The (2R)-stereochemistry provides defined stereocontrol in downstream transformations, making it valuable for medicinal chemistry and process-oriented synthesis.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P341-P312-P330-P363-P501
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Lot numbers can be found on the outside label of a product: