(S)-N-Fmoc-2-(4'-pentenyl)glycine

98%

Reagent Code: #235144
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CAS Number 856412-22-1

science Other reagents with same CAS 856412-22-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 365.42 g/mol
Formula C₂₂H₂₃NO₄
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in solid-phase peptide synthesis as a chiral building block for introducing a side chain with a terminal alkene functionality. The Fmoc group allows for mild base-labile protection during stepwise synthesis, enabling the construction of complex peptides with site-specific modifications. The pentenyl side chain serves as a handle for post-assembly functionalization, such as thiol-ene coupling or ring-closing metathesis, useful in peptide cyclization or conjugation to carriers, surfaces, or labels. Particularly valuable in developing peptide-based therapeutics, probes, and biomaterials where precise control over structure and functionalization is required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,540.00
inventory 1g
10-20 days ฿6,680.00
inventory 5g
10-20 days ฿27,430.00
inventory 25g
10-20 days ฿96,260.00
inventory 250mg
10-20 days ฿2,390.00
(S)-N-Fmoc-2-(4'-pentenyl)glycine
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Used in solid-phase peptide synthesis as a chiral building block for introducing a side chain with a terminal alkene functionality. The Fmoc group allows for mild base-labile protection during stepwise synthesis, enabling the construction of complex peptides with site-specific modifications. The pentenyl side chain serves as a handle for post-assembly functionalization, such as thiol-ene coupling or ring-closing metathesis, useful in peptide cyclization or conjugation to carriers, surfaces, or labels. Pa

Used in solid-phase peptide synthesis as a chiral building block for introducing a side chain with a terminal alkene functionality. The Fmoc group allows for mild base-labile protection during stepwise synthesis, enabling the construction of complex peptides with site-specific modifications. The pentenyl side chain serves as a handle for post-assembly functionalization, such as thiol-ene coupling or ring-closing metathesis, useful in peptide cyclization or conjugation to carriers, surfaces, or labels. Particularly valuable in developing peptide-based therapeutics, probes, and biomaterials where precise control over structure and functionalization is required.

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