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

>97%

Reagent Code: #235140
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CAS Number 288617-73-2

science Other reagents with same CAS 288617-73-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 379.45 g/mol
Formula C₂₃H₂₅NO₄
inventory_2 Storage & Handling
Storage −20°C

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 orthogonal protection, enabling stepwise assembly of peptides under mild basic conditions. The pentenyl side chain serves as a handle for post-assembly modifications, such as thiol-ene coupling or metathesis reactions, useful in peptide cyclization, bioconjugation, or attachment to surfaces and polymers. Commonly applied in the development of peptide-based therapeutics, probes, and biomaterials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿187.00
inventory 250mg
10-20 days ฿440.00
inventory 5g
10-20 days ฿11,460.00
inventory 1g
10-20 days ฿2,380.00

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(S)-N-Fmoc-2-(4'-pentenyl)alanine
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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 orthogonal protection, enabling stepwise assembly of peptides under mild basic conditions. The pentenyl side chain serves as a handle for post-assembly modifications, such as thiol-ene coupling or metathesis reactions, useful in peptide cyclization, bioconjugation, or attachment to surfaces and polymers. Commonly applied in the development of peptide-b
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 orthogonal protection, enabling stepwise assembly of peptides under mild basic conditions. The pentenyl side chain serves as a handle for post-assembly modifications, such as thiol-ene coupling or metathesis reactions, useful in peptide cyclization, bioconjugation, or attachment to surfaces and polymers. Commonly applied in the development of peptide-based therapeutics, probes, and biomaterials.
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