(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(((tert-butoxycarbonyl)amino)methyl)phenyl)propanoic acid

97%

  • Product Code: 104327
  CAS:    204715-91-3
Molecular Weight: 516.58 g./mol Molecular Formula: C₃₀H₃₂N₂O₆
EC Number: MDL Number: MFCD01317015
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
Product Description: This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group, while the tert-butoxycarbonyl (Boc) group safeguards the side-chain amino functionality. This dual protection allows for selective deprotection during peptide chain assembly, ensuring precise control over the synthesis process. It is especially valuable in producing peptides for pharmaceutical research, drug development, and biochemical studies, where high purity and specific sequences are critical.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days Ft13,866.28
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0.250 10-20 days Ft24,532.64
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1.000 10-20 days Ft90,470.18
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-
5.000 10-20 days Ft436,254.41
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-
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(((tert-butoxycarbonyl)amino)methyl)phenyl)propanoic acid
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group, while the tert-butoxycarbonyl (Boc) group safeguards the side-chain amino functionality. This dual protection allows for selective deprotection during peptide chain assembly, ensuring precise control over the synthesis process. It is especially valuable in producing peptides for pharmaceutical research, drug development, and biochemical studies, where high purity and specific sequences are critical.
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