(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%

  • Product Code: 236514
  CAS:    1662688-20-1
Molecular Weight: 1196.51 g./mol Molecular Formula: C₆₄H₁₀₁N₅O₁₆
EC Number: MDL Number: MFCD33551739
Melting Point: Boiling Point:
Density: Storage Condition: -20°C, dry
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.
Sizes / Availability / Pricing:
Size Availability Price Quantity
100mg 10-20 days ฿1,320.00
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250mg 10-20 days ฿2,290.00
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1g 10-20 days ฿6,450.00
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(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
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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