N-Fmoc-2-amino-2-(2-propenyl)-4-Pentenoicacid,

97%

Reagent Code: #217382
label
Alias 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-allyl-4-enic acid
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CAS Number 1311992-97-8

science Other reagents with same CAS 1311992-97-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 377.44 g/mol
Formula C₂₃H₂₃NO₄
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in solid-phase peptide synthesis as a protected amino acid building block, particularly for incorporating unsaturated side chains into peptide structures. The Fmoc group allows for mild base-labile protection, compatible with stepwise elongation on resin. The allyl and pentenoyl moieties provide sites for post-assembly modifications, such as ring-closing metathesis, enabling the formation of cyclic peptides or constrained architectures. Commonly applied in the synthesis of bioactive peptide analogs and peptidomimetics where structural rigidity or specific side-chain functionality is required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,060.00
inventory 250mg
10-20 days ฿5,200.00
inventory 1g
10-20 days ฿14,000.00
inventory 5g
10-20 days ฿53,060.00
N-Fmoc-2-amino-2-(2-propenyl)-4-Pentenoicacid,
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Used in solid-phase peptide synthesis as a protected amino acid building block, particularly for incorporating unsaturated side chains into peptide structures. The Fmoc group allows for mild base-labile protection, compatible with stepwise elongation on resin. The allyl and pentenoyl moieties provide sites for post-assembly modifications, such as ring-closing metathesis, enabling the formation of cyclic peptides or constrained architectures. Commonly applied in the synthesis of bioactive peptide analogs

Used in solid-phase peptide synthesis as a protected amino acid building block, particularly for incorporating unsaturated side chains into peptide structures. The Fmoc group allows for mild base-labile protection, compatible with stepwise elongation on resin. The allyl and pentenoyl moieties provide sites for post-assembly modifications, such as ring-closing metathesis, enabling the formation of cyclic peptides or constrained architectures. Commonly applied in the synthesis of bioactive peptide analogs and peptidomimetics where structural rigidity or specific side-chain functionality is required.

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