(23S, 50S)-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-23-(tert-butoxycarbonyl)-2, 2-dimethyl-4, 21, 26, 35, 44-pentaoxo-3, 30, 33, 39, 42-pentaoxa-22, 27, 36, 45-tetraazahenpentacontan-51-oic acid

98%

Reagent Code: #236514
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CAS Number 1662688-20-1

science Other reagents with same CAS 1662688-20-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1196.51 g/mol
Formula C₆₄H₁₀₁N₅O₁₆
badge Registry Numbers
MDL Number MFCD33551739
inventory_2 Storage & Handling
Storage -20°C, dry

description Product Description

Used primarily in solid-phase peptide synthesis as a protected amino acid building block. Its Fmoc group allows for mild base-labile deprotection, enabling stepwise assembly of peptides without affecting other protecting groups. The tert-butoxycarbonyl (Boc) protection on the side chain provides orthogonal stability during synthesis, making it suitable for complex peptide sequences. The polyether and ester linkages enhance solubility in common organic solvents, improving coupling efficiency. Widely applied in the preparation of structured peptides, peptide conjugates, and peptidomimetics for pharmaceutical and biochemical research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,320.00
inventory 250mg
10-20 days ฿2,290.00
inventory 1g
10-20 days ฿6,450.00
(23S, 50S)-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-23-(tert-butoxycarbonyl)-2, 2-dimethyl-4, 21, 26, 35, 44-pentaoxo-3, 30, 33, 39, 42-pentaoxa-22, 27, 36, 45-tetraazahenpentacontan-51-oic acid
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Used primarily in solid-phase peptide synthesis as a protected amino acid building block. Its Fmoc group allows for mild base-labile deprotection, enabling stepwise assembly of peptides without affecting other protecting groups. The tert-butoxycarbonyl (Boc) protection on the side chain provides orthogonal stability during synthesis, making it suitable for complex peptide sequences. The polyether and ester linkages enhance solubility in common organic solvents, improving coupling efficiency. Widely appli

Used primarily in solid-phase peptide synthesis as a protected amino acid building block. Its Fmoc group allows for mild base-labile deprotection, enabling stepwise assembly of peptides without affecting other protecting groups. The tert-butoxycarbonyl (Boc) protection on the side chain provides orthogonal stability during synthesis, making it suitable for complex peptide sequences. The polyether and ester linkages enhance solubility in common organic solvents, improving coupling efficiency. Widely applied in the preparation of structured peptides, peptide conjugates, and peptidomimetics for pharmaceutical and biochemical research.

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