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Structure of 151978-50-6
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N-Boc-4-pentyne-1-amine features a terminal alkyne group flanked by a primary amine protected as a Boc carbamate. This bifunctional scaffold enables efficient conjugation via click chemistry and offers enhanced stability during handling. The electron-deficient alkyne facilitates rapid copper-catalyzed cycloadditions, while the bench-stable Boc protection simplifies purification and storage.
N-Boc-4-pentyne-1-amine serves as a versatile building block for the synthesis of alkynyl-containing heterocycles and bioactive molecules. Its terminal alkyne functionality enables reliable copper-catalyzed azide-alkyne cycloaddition (CuAAC), while the Boc-protected amine offers stability and orthogonal reactivity. The molecule exhibits excellent bench stability, facilitates straightforward purification, and functions effectively in standard coupling and cyclization protocols.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3259
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H314
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Precautionary Statements : P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: