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Catalog Number:
01915
Fmoc-O-tert-butyl-L-tyrosine 4-alkoxybenzyl alcohol resin
Synonym(s):
Fmoc-L-Tyr(tBu)-Wang resin
Documents
$34.85 /1G
Pack Size Availability Price
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Product Information

Fmoc-O-tert-butyl-L-tyrosine 4-alkoxybenzyl alcohol is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This derivative of L-tyrosine features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which allows for selective deprotection during the synthesis process, making it an essential building block for researchers in the field of organic chemistry. Its unique structure not only enhances solubility but also provides stability during various reactions, facilitating the creation of complex peptide sequences.

This compound is particularly valuable in the development of pharmaceuticals, where precise control over peptide synthesis is crucial. It has been employed in the design of bioactive peptides, which can serve as potential therapeutic agents in treating various diseases. Additionally, the incorporation of the 4-alkoxybenzyl alcohol moiety can enhance the compound's reactivity and compatibility with other functional groups, making it a preferred choice for chemists looking to streamline their synthesis processes. With its robust properties and practical applications, Fmoc-O-tert-butyl-L-tyrosine 4-alkoxybenzyl alcohol stands out as a key reagent in modern chemical research.

Synonyms
Fmoc-L-Tyr(tBu)-Wang resin
MDL Number
MFCD00801270
Appearance
Pale to yellow beads
Substitution
0.3 - 0.8 mmol/g
Mesh Size
100 - 200 mesh
Conditions
Store at 0 - 8 °C
%DVB
1% DVB
General Information
Synonyms
Fmoc-L-Tyr(tBu)-Wang resin
MDL Number
MFCD00801270
Appearance
Pale to yellow beads
Substitution
0.3 - 0.8 mmol/g
Mesh Size
100 - 200 mesh
Conditions
Store at 0 - 8 °C
%DVB
1% DVB
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-O-tert-butyl-L-tyrosine 4-alkoxybenzyl alcohol 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 creation of complex and functional peptide sequences.
  • Drug Development: It is employed in the development of pharmaceutical compounds, especially those targeting specific receptors, enhancing the efficacy and selectivity of drug candidates.
  • Bioconjugation: The chemical is used in bioconjugation techniques, facilitating the attachment of biomolecules to drugs or imaging agents, which is crucial for targeted therapy and diagnostics.
  • Research in Neuroscience: Its derivatives are explored in neuroscience research for studying neurotransmitter pathways and developing neuroprotective agents.
  • Cosmetic Formulations: The compound finds applications in cosmetic chemistry, particularly in formulations aimed at skin rejuvenation and anti-aging, due to its potential beneficial effects on skin cells.

Citations