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Catalog Number:
05702
CAS Number:
214750-75-1
N-Fmoc-N-allyloxycarbonyl-D-lysine
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-Nε-allyloxycarbonyl-D-lysine
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Product Information

Na-Fmoc-Ne-allyloxycarbonyl-D-lysine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which facilitates the selective modification of amino acids during solid-phase peptide synthesis. Its unique allyloxycarbonyl group enhances its reactivity, making it an excellent choice for researchers looking to introduce specific functionalities into peptides. The compound's stability under various conditions allows for efficient coupling reactions, making it a preferred choice in the synthesis of complex peptides and bioactive molecules.

In addition to its role in peptide synthesis, Na-Fmoc-Ne-allyloxycarbonyl-D-lysine is also valuable in the development of therapeutic agents and bioconjugates. Its ability to form stable linkages with other biomolecules opens avenues for creating targeted drug delivery systems and novel therapeutics. Researchers in medicinal chemistry and biochemistry will find this compound particularly beneficial for its ease of use and the potential to streamline the synthesis of intricate peptide structures, ultimately accelerating the pace of discovery in drug development.

Synonyms
Fmoc-Nε-allyloxycarbonyl-D-lysine
CAS Number
214750-75-1
Purity
≥ 98% (HPLC)
Molecular Formula
C25H28N2O6
Molecular Weight
452.51
MDL Number
MFCD00798639
PubChem ID
3899900
Melting Point
91 - 112 °C
Appearance
White powder
Optical Rotation
[a]D20 = +13 ± 2 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-Nε-allyloxycarbonyl-D-lysine
CAS Number
214750-75-1
Purity
≥ 98% (HPLC)
Molecular Formula
C25H28N2O6
Molecular Weight
452.51
MDL Number
MFCD00798639
PubChem ID
3899900
Melting Point
91 - 112 °C
Appearance
White powder
Optical Rotation
[a]D20 = +13 ± 2 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Fmoc-Ne-allyloxycarbonyl-D-lysine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions and enhancing the yield of desired products. Its stability under various conditions makes it a preferred choice for chemists.
  • Drug Development: In medicinal chemistry, it is used to modify amino acids in drug candidates, improving their bioavailability and efficacy. This application is crucial for developing new therapeutics.
  • Bioconjugation: It facilitates the conjugation of biomolecules, such as proteins and antibodies, which is essential in creating targeted drug delivery systems and diagnostic tools.
  • Research in Neuroscience: The compound is employed in studies involving neuropeptides, helping researchers understand neurological functions and disorders, which can lead to innovative treatments.
  • Custom Synthesis: Its versatility allows for the tailored synthesis of various derivatives, catering to specific research needs in academic and industrial laboratories.

Citations