(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-8-(allyloxy)-8-oxooctanoic acid

95%

Reagent Code: #232837
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CAS Number 167368-90-3

science Other reagents with same CAS 167368-90-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 451.51 g/mol
Formula C₂₆H₂₉NO₆
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in peptide synthesis as a protected amino acid building block. The Fmoc group enables solid-phase peptide synthesis by providing reversible protection for the amino group, allowing stepwise assembly of peptides under mild basic conditions. The allyloxy moiety on the side chain acts as an orthogonal protecting group, which can be selectively removed in the presence of other protecting groups, enabling precise control during complex peptide synthesis. Commonly employed in the preparation of long or modified peptides, including those used in pharmaceutical research and development. Its solubility in common organic solvents facilitates handling in automated synthesizers.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿20,000.00
(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-8-(allyloxy)-8-oxooctanoic acid
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Used primarily in peptide synthesis as a protected amino acid building block. The Fmoc group enables solid-phase peptide synthesis by providing reversible protection for the amino group, allowing stepwise assembly of peptides under mild basic conditions. The allyloxy moiety on the side chain acts as an orthogonal protecting group, which can be selectively removed in the presence of other protecting groups, enabling precise control during complex peptide synthesis. Commonly employed in the preparation of

Used primarily in peptide synthesis as a protected amino acid building block. The Fmoc group enables solid-phase peptide synthesis by providing reversible protection for the amino group, allowing stepwise assembly of peptides under mild basic conditions. The allyloxy moiety on the side chain acts as an orthogonal protecting group, which can be selectively removed in the presence of other protecting groups, enabling precise control during complex peptide synthesis. Commonly employed in the preparation of long or modified peptides, including those used in pharmaceutical research and development. Its solubility in common organic solvents facilitates handling in automated synthesizers.

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