(2R,3S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(benzyloxy)butanoic acid

≥95%

  • Product Code: 50252
  CAS:    131545-63-6
Molecular Weight: 431.48 g./mol Molecular Formula: C₂₆H₂₅NO₅
EC Number: MDL Number: MFCD00237033
Melting Point: Boiling Point: 643.7°C at 760 mmHg
Density: Storage Condition: Room temperature, dry and sealed
Product Description: This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block in solid-phase peptide synthesis (SPPS), where the fluorenylmethoxycarbonyl (Fmoc) group acts as a temporary protecting group for the amino functionality. The benzyloxy group protects the hydroxyl side chain, ensuring selective reactivity during the coupling process. Its application is crucial in producing peptides with high purity and specificity, particularly in pharmaceutical research and drug development. The compound’s structure allows for efficient deprotection and coupling steps, making it a valuable tool in synthesizing complex peptides and proteins.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $14.95
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0.250 10-20 days $16.07
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1.000 10-20 days $38.12
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5.000 10-20 days $121.85
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(2R,3S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(benzyloxy)butanoic acid
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block in solid-phase peptide synthesis (SPPS), where the fluorenylmethoxycarbonyl (Fmoc) group acts as a temporary protecting group for the amino functionality. The benzyloxy group protects the hydroxyl side chain, ensuring selective reactivity during the coupling process. Its application is crucial in producing peptides with high purity and specificity, particularly in pharmaceutical research and drug development. The compound’s structure allows for efficient deprotection and coupling steps, making it a valuable tool in synthesizing complex peptides and proteins.
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