2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(but-3-en-1-yl)hex-5-enoic acid

97%

Reagent Code: #194782
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CAS Number 1311992-98-9

science Other reagents with same CAS 1311992-98-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 405.49 g/mol
Formula C₂₅H₂₇NO₄
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Widely used in peptide synthesis as a protected amino acid building block, this compound enables the introduction of reactive alkene side chains into peptide sequences. The Fmoc group provides orthogonal protection for the alpha-amino function, allowing stepwise assembly of peptides under mild basic conditions. The terminal alkenes on the side chain and main chain offer sites for post-synthetic modifications via thiol-ene chemistry or cross-metathesis, making it valuable for preparing functionalized peptides, peptide conjugates, or hydrogels. Its design supports solid-phase synthesis and is particularly useful in developing peptide-based biomaterials and bioconjugates.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿275.00
inventory 100mg
10-20 days ฿533.50
inventory 250mg
10-20 days ฿1,570.00
inventory 1g
10-20 days ฿4,000.00

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2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(but-3-en-1-yl)hex-5-enoic acid
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Widely used in peptide synthesis as a protected amino acid building block, this compound enables the introduction of reactive alkene side chains into peptide sequences. The Fmoc group provides orthogonal protection for the alpha-amino function, allowing stepwise assembly of peptides under mild basic conditions. The terminal alkenes on the side chain and main chain offer sites for post-synthetic modifications via thiol-ene chemistry or cross-metathesis, making it valuable for preparing functionalized peptides, peptide conjugates, or hydrogels. Its design supports solid-phase synthesis and is particularly useful in developing peptide-based biomaterials and bioconjugates.
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