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Catalog Number:
29650
CAS Number:
1204595-05-0
Fmoc-L-Tyr(propargyl)-OH
Purity:
≥ 99 % (HPLC)
Documents
$65.40 /100 mg
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Product Information

Fmoc-L-Tyr(propargyl)-OH is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely recognized for its stability and ease of removal under mild conditions, making it an ideal choice for researchers focused on solid-phase peptide synthesis. The propargyl group enhances its utility in click chemistry applications, allowing for efficient conjugation reactions that are essential in the development of bioconjugates and targeted therapeutics.

This compound is particularly valuable in the fields of medicinal chemistry and biochemistry, where it can be utilized to create novel peptide-based drugs or as a building block in the synthesis of complex biomolecules. Its unique structure not only facilitates the incorporation of functional groups but also provides opportunities for the development of innovative therapeutic agents. Researchers can leverage the properties of Fmoc-L-Tyr(propargyl)-OH to explore new avenues in drug design and delivery, making it a significant addition to any chemical toolkit.

CAS Number
1204595-05-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C 27 H 235
Molecular Weight
441.48
MDL Number
MFCD26793610
PubChem ID
90122665
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
General Information
CAS Number
1204595-05-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C 27 H 235
Molecular Weight
441.48
MDL Number
MFCD26793610
PubChem ID
90122665
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-L-Tyr(propargyl)-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound is a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the introduction of unique functionalities.
  • Drug Development: Its propargyl group can facilitate the creation of novel drug candidates, especially in the development of targeted therapies for various diseases.
  • Bioconjugation: The compound's reactive alkyne group enables efficient bioconjugation techniques, which are essential in creating targeted delivery systems in pharmaceuticals.
  • Research in Neuroscience: It is used in the synthesis of compounds that can modulate neurotransmitter systems, aiding in the study of neurological disorders.
  • Materials Science: The unique properties of this compound allow for its application in developing functional materials, such as sensors or drug delivery systems, enhancing performance compared to traditional compounds.

Citations