6-Azido-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-norleucine

98%

  • Product Code: 65209
  CAS:    159610-89-6
Molecular Weight: 394.43 g./mol Molecular Formula: C₂₁H₂₂N₄O₄
EC Number: MDL Number: MFCD13182319
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
Product Description: This compound is primarily utilized in peptide synthesis and bioconjugation processes. It serves as a building block for introducing azide functionalities into peptides, which are essential for click chemistry reactions. The azide group enables efficient and selective coupling with alkyne-containing molecules, facilitating the creation of complex biomolecular structures. Additionally, the fluorenylmethoxycarbonyl (Fmoc) protecting group ensures controlled deprotection during solid-phase peptide synthesis, enhancing precision in peptide chain assembly. Its application is particularly valuable in drug development, protein engineering, and the study of biomolecular interactions, where site-specific modifications are crucial.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.050 10-20 days $50.63
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-
0.250 10-20 days $143.75
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6-Azido-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-norleucine
This compound is primarily utilized in peptide synthesis and bioconjugation processes. It serves as a building block for introducing azide functionalities into peptides, which are essential for click chemistry reactions. The azide group enables efficient and selective coupling with alkyne-containing molecules, facilitating the creation of complex biomolecular structures. Additionally, the fluorenylmethoxycarbonyl (Fmoc) protecting group ensures controlled deprotection during solid-phase peptide synthesis, enhancing precision in peptide chain assembly. Its application is particularly valuable in drug development, protein engineering, and the study of biomolecular interactions, where site-specific modifications are crucial.
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