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Structure of 1217669-02-7
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Fmoc-S-3-amino-5-hexynic acid integrates a terminal alkyne and primary amine for bioorthogonal conjugation. This bifunctional reagent enables site-specific labeling via CuAAC or strain-promoted reactions, combining high reactivity with stability under standard conditions. The Fmoc group facilitates efficient solid-phase synthesis and protection of the amine.
Fmoc-S-3-amino-5-hexynic acid serves as a versatile building block for the synthesis of peptidomimetics and bioconjugates. Its terminal alkyne enables efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC), while the Fmoc-protected amine and carboxylic acid facilitate standard solid-phase peptide synthesis. The molecule exhibits excellent bench stability, ease of purification, and compatibility with diverse functional groups, making it ideal for constructing complex scaffolds in medicinal chemistry and chemical biology workflows.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: