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*For research and further manufacturing use only, not for direct human use.
Structure of 945212-26-0
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Fmoc-(R)-2-(7-octenyl)Ala-OH features a terminal alkene handle for site-specific conjugation, enabling efficient bioorthogonal functionalization in peptide synthesis. The bench-stable, moisture-tolerant side chain integrates seamlessly into solid-phase workflows, offering a robust platform for generating tailored peptide architectures with enhanced structural diversity and compatibility.
Fmoc-(R)-2-(7-octenyl)Ala-OH serves as a versatile amino acid building block for solid-phase peptide synthesis, enabling the incorporation of a hydrophobic alkenyl side chain at the β-position. The pendant 7-octenyl group provides a handle for post-functionalization via click chemistry or transition-metal-catalyzed coupling, enhancing structural diversity in peptidomimetics and macrocyclic scaffolds. Bench-stable and readily purified by standard chromatography, it functions effectively in both academic and industrial workflows.
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GHS Pictogram :
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GHS No : GHS09
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Signal Word : Warning
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H410
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Precautionary Statements : P273-P391-P501
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Lot numbers can be found on the outside label of a product: