(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(1-(tert-butoxycarbonyl)-1H-indol-3-yl)propanoic acid

97%

  • Product Code: 97576
  CAS:    197632-75-0
Molecular Weight: 540.61 g./mol Molecular Formula: C₃₂H₃₂N₂O₆
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: room temperature, dry
Product Description: This chemical is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group protects the amino functionality, and the tert-butoxycarbonyl (Boc) group protects the indole nitrogen of the tryptophan side chain. This dual protection strategy allows for selective deprotection during the stepwise assembly of peptides, ensuring the integrity and specificity of the synthesis process. It is especially valuable in the synthesis of complex peptides containing tryptophan residues, as it prevents unwanted side reactions and enhances yield and purity. Its application is critical in pharmaceutical research, biotechnology, and the development of peptide-based therapeutics.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.050 10-20 days ฿792.00
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0.250 10-20 days ฿2,205.00
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1.000 10-20 days ฿6,102.00
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(1-(tert-butoxycarbonyl)-1H-indol-3-yl)propanoic acid
This chemical is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group protects the amino functionality, and the tert-butoxycarbonyl (Boc) group protects the indole nitrogen of the tryptophan side chain. This dual protection strategy allows for selective deprotection during the stepwise assembly of peptides, ensuring the integrity and specificity of the synthesis process. It is especially valuable in the synthesis of complex peptides containing tryptophan residues, as it prevents unwanted side reactions and enhances yield and purity. Its application is critical in pharmaceutical research, biotechnology, and the development of peptide-based therapeutics.
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