(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-(1,3-dioxoisoindolin-2-yl)hexanoic acid

98%

Reagent Code: #233631
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CAS Number 83999-93-3

science Other reagents with same CAS 83999-93-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 498.53 g/mol
Formula C₂₉H₂₆N₂O₆
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in peptide synthesis as a protected amino acid building block, this compound enables the incorporation of a lysine derivative bearing a phthaloyl-protected side chain amine. The Fmoc group allows for orthogonal protection, facilitating stepwise assembly of peptides under mild basic conditions, commonly in solid-phase synthesis. The phthaloyl moiety stabilizes the side chain during chain elongation and can be selectively removed later to enable side-chain modifications, such as acetylation or biotinylation. Its structure supports the synthesis of complex peptides and proteins, especially those requiring post-translational modifications at lysine residues. Widely applied in research settings for developing therapeutic peptides, biochemical probes, and diagnostic agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,360.00
inventory 250mg
10-20 days ฿7,390.00
inventory 1g
10-20 days ฿19,950.00
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-(1,3-dioxoisoindolin-2-yl)hexanoic acid
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Used primarily in peptide synthesis as a protected amino acid building block, this compound enables the incorporation of a lysine derivative bearing a phthaloyl-protected side chain amine. The Fmoc group allows for orthogonal protection, facilitating stepwise assembly of peptides under mild basic conditions, commonly in solid-phase synthesis. The phthaloyl moiety stabilizes the side chain during chain elongation and can be selectively removed later to enable side-chain modifications, such as acetylation or biotinylation. Its structure supports the synthesis of complex peptides and proteins, especially those requiring post-translational modifications at lysine residues. Widely applied in research settings for developing therapeutic peptides, biochemical probes, and diagnostic agents.
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