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Catalog Number:
16879
CAS Number:
1217835-37-4
Fmoc- O -allyl-D- m -tyrosine
Purity:
≥ 99,5 % (HPLC chirale)
Synonym(s):
Fmoc-D- m -Tyr(Tous)-OH, Fmoc-D-3-allyloxyphénylalanine
Documents
$100.05 /100 mg
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Product Information

Fmoc-O-allyl-D-m-tyrosine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique allyl side chain enhances its reactivity, making it an excellent choice for researchers focusing on the development of novel therapeutic peptides. The compound's structural properties allow for efficient coupling reactions, facilitating the formation of complex peptide sequences with high purity and yield.

In addition to its applications in peptide synthesis, Fmoc-O-allyl-D-m-tyrosine is also valuable in the study of protein interactions and structure-function relationships. Its ability to incorporate into peptides without disrupting their biological activity makes it a preferred choice for researchers exploring drug design and biomolecular studies. The compound's stability and compatibility with various coupling reagents further enhance its utility in laboratory settings, providing researchers with a reliable tool for advancing their projects.

Synonyms
Fmoc-D- m -Tyr(Tous)-OH, Fmoc-D-3-allyloxyphénylalanine
CAS Number
1217835-37-4
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 27 H 255
Molecular Weight
443.49
MDL Number
MFCD08061621
PubChem ID
53398476
Melting Point
96 - 102 ºC
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20 = 30 ± 1 º (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-D- m -Tyr(Tous)-OH, Fmoc-D-3-allyloxyphénylalanine
CAS Number
1217835-37-4
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 27 H 255
Molecular Weight
443.49
MDL Number
MFCD08061621
PubChem ID
53398476
Melting Point
96 - 102 ºC
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20 = 30 ± 1 º (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-O-allyl-D-m-tyrosine 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. Its protective group allows for selective reactions, enhancing the efficiency of creating complex peptides.
  • Drug Development: In pharmaceutical research, it is used to develop peptide-based drugs. The unique properties of this compound can lead to improved bioavailability and specificity in drug action.
  • Bioconjugation: The allyl group facilitates bioconjugation processes, allowing researchers to attach various biomolecules, such as antibodies or enzymes, to peptides. This is crucial in creating targeted therapies and diagnostic tools.
  • Research in Neuroscience: It can be employed in studies related to neurotransmitter functions, as modified tyrosine residues are important in the synthesis of neurotransmitters like dopamine, aiding in the understanding of neurological disorders.
  • Materials Science: The compound's unique structure can be utilized in the development of novel materials, such as hydrogels or drug delivery systems, providing enhanced performance in biomedical applications.

Citations