🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
16880
CAS Number:
1175973-95-1
Fmoc-O-allyl-L-m-tyrosine
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-L-m-Tyr(All)-OH, Fmoc-L-3-Allyloxyphenylalanine, Fmoc-m-Tyr(All)-OH
Documents
$90.60 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Fmoc-O-allyl-L-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 the compound's reactivity and provides opportunities for further functionalization, making it an attractive choice for researchers focused on developing novel therapeutic agents.

In the pharmaceutical industry, Fmoc-O-allyl-L-m-tyrosine is particularly valuable for the synthesis of bioactive peptides and proteins, which are crucial in drug discovery and development. Its ability to facilitate the incorporation of modified amino acids into peptides allows for the exploration of new biological activities and therapeutic potentials. Researchers can leverage this compound to create targeted therapies, improve drug efficacy, and enhance the stability of peptide-based drugs. With its favorable properties and applications, Fmoc-O-allyl-L-m-tyrosine stands out as a key building block for innovative research and development in the life sciences.

Synonyms
Fmoc-L-m-Tyr(All)-OH, Fmoc-L-3-Allyloxyphenylalanine, Fmoc-m-Tyr(All)-OH
CAS Number
1175973-95-1
Purity
≥ 99% (HPLC)
Molecular Formula
C27H25NO5
Molecular Weight
443.49
MDL Number
MFCD08061623
PubChem ID
53398476
Melting Point
104 - 111 °C (Lit.)
Appearance
White solid
Optical Rotation
[a]D20 = -28.5 ± 3 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-m-Tyr(All)-OH, Fmoc-L-3-Allyloxyphenylalanine, Fmoc-m-Tyr(All)-OH
CAS Number
1175973-95-1
Purity
≥ 99% (HPLC)
Molecular Formula
C27H25NO5
Molecular Weight
443.49
MDL Number
MFCD08061623
PubChem ID
53398476
Melting Point
104 - 111 °C (Lit.)
Appearance
White solid
Optical Rotation
[a]D20 = -28.5 ± 3 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-O-allyl-L-m-tyrosine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create specific sequences for various applications in drug development and biotechnology.
  • Drug Development: Its unique structure enhances the solubility and stability of peptide-based drugs, making it a valuable component in the pharmaceutical industry for formulating effective medications.
  • Bioconjugation: The allyl group facilitates bioconjugation processes, enabling the attachment of biomolecules to surfaces or other compounds, which is crucial in creating targeted therapies and diagnostics.
  • Research in Neuroscience: This compound is used in studies related to neuropeptides, helping scientists understand their roles in neurological functions and potential treatments for neurodegenerative diseases.
  • Customizable Chemical Libraries: Fmoc-O-allyl-L-m-tyrosine is integral in generating diverse chemical libraries for screening potential drug candidates, providing researchers with a versatile tool for innovation.

Citations