Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
31668
CAS Number:
1145678-51-8
Fmoc-L-Tyr(3-Me)-OH
Purity:
≥ 99 % (HPLC)
Documents
$65.40 /25 mg
Tamaño
Request Bulk Quote
Product Information

Fmoc-L-Tyr(3-Me)-OH 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 amine functionalities during the synthesis of complex peptides. Its unique structure, characterized by a 4-hydroxy-3-methylphenyl side chain, enhances its solubility and reactivity, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry.

In practical applications, Fmoc-L-Tyr(3-Me)-OH is commonly employed in solid-phase peptide synthesis (SPPS), where its stability under various conditions allows for the efficient assembly of peptides. This compound's ability to facilitate the incorporation of tyrosine residues into peptides can lead to the development of novel therapeutics, particularly in the design of peptide-based drugs with enhanced bioactivity. Researchers appreciate its reliability and effectiveness, making it a preferred choice for those looking to innovate in peptide chemistry.

CAS Number
1145678-51-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 25 H 23 N º 5
Molecular Weight
417.46
MDL Number
MFCD30749167
PubChem ID
138108833
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -20 ± 2 º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
1145678-51-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C 25 H 23 N º 5
Molecular Weight
417.46
MDL Number
MFCD30749167
PubChem ID
138108833
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -20 ± 2 º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-L-Tyr(3-Me)-OH 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 researchers to create complex proteins efficiently.
  • Drug Development: Its unique structure makes it valuable in the pharmaceutical industry for developing new drugs, especially those targeting specific biological pathways related to cancer and neurological disorders.
  • Bioconjugation: The compound is used in bioconjugation techniques, enabling the attachment of biomolecules to drugs or imaging agents, enhancing their efficacy and specificity in therapeutic applications.
  • Research in Neuroscience: Due to its structural similarities to neurotransmitters, it is employed in neuroscience research to study receptor interactions and the effects of modified amino acids on brain function.
  • Cosmetic Formulations: The compound is explored in cosmetic chemistry for its potential benefits in skin care products, particularly for formulations aimed at improving skin hydration and elasticity.

Citas