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Catalog Number:
07048
CAS Number:
221884-63-5
Fmoc-a-allyl-DL-glycine
Purity:
≥ 99%
Synonym(s):
Fmoc-DL-Gly(α-allyl)-OH, Fmoc-DL-2-amino-4-pentenoic acid
Documents
$72.31 /250MG
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Product Information

Fmoc-a-allyl-DL-glycine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which facilitates the selective modification of amino acids during solid-phase peptide synthesis. Its unique allyl side chain enhances the compound's reactivity, making it an excellent choice for researchers looking to introduce specific functionalities into peptides.

In addition to its role in peptide synthesis, Fmoc-a-allyl-DL-glycine can be employed in the development of novel therapeutic agents, particularly in the fields of medicinal chemistry and biochemistry. Its ability to undergo various coupling reactions allows for the creation of complex peptide structures, which are essential in the design of biologically active compounds. Researchers benefit from its stability and compatibility with a range of coupling reagents, making it a valuable tool in the synthesis of custom peptides for pharmaceutical applications.

Synonyms
Fmoc-DL-Gly(α-allyl)-OH, Fmoc-DL-2-amino-4-pentenoic acid
CAS Number
221884-63-5
Purity
≥ 99%
Molecular Formula
C20H19NO4
Molecular Weight
337.42
MDL Number
MFCD02259489
PubChem ID
4052587
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-DL-Gly(α-allyl)-OH, Fmoc-DL-2-amino-4-pentenoic acid
CAS Number
221884-63-5
Purity
≥ 99%
Molecular Formula
C20H19NO4
Molecular Weight
337.42
MDL Number
MFCD02259489
PubChem ID
4052587
Appearance
White powder
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

Fmoc-a-allyl-DL-glycine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the incorporation of unique functionalities that enhance peptide properties.
  • Drug Development: Its structural characteristics make it valuable in the design of novel pharmaceuticals, especially in creating compounds with improved bioactivity and selectivity.
  • Bioconjugation: The allyl group facilitates bioconjugation reactions, enabling researchers to attach biomolecules to surfaces or other molecules, which is crucial in developing targeted drug delivery systems.
  • Research in Neuroscience: It can be used to study neuropeptides and their interactions, contributing to advancements in understanding neurological disorders and potential treatments.
  • Material Science: The compound's unique properties allow it to be used in developing advanced materials, such as hydrogels, which can be applied in tissue engineering and regenerative medicine.

Citations