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Catalog Number:
24177
CAS Number:
247088-44-4
N-(Tert-Butoxycarbonyl)-O-Ethyltyrosine
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$103.56 /250MG
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Product Information

N-(Tert-Butoxycarbonyl)-O-Ethyltyrosine is a versatile compound widely utilized in the field of organic synthesis and pharmaceutical research. This compound, also known as Boc-O-Et-Tyr, serves as a valuable building block in the development of peptide-based therapeutics and drug candidates. Its unique tert-butoxycarbonyl (Boc) protective group allows for selective deprotection under mild conditions, making it an ideal choice for researchers looking to synthesize complex molecules with precision.

In addition to its role in peptide synthesis, N-(Tert-Butoxycarbonyl)-O-Ethyltyrosine has shown potential in the development of novel drug formulations, particularly in enhancing the bioavailability of therapeutic agents. Its ethoxy group contributes to improved solubility, which is crucial for effective drug delivery. Researchers in medicinal chemistry and biochemistry will find this compound particularly beneficial for creating targeted therapies and studying the structure-activity relationships of tyrosine derivatives. With its favorable properties and applications, N-(Tert-Butoxycarbonyl)-O-Ethyltyrosine stands out as a key reagent for advancing pharmaceutical innovations.

CAS Number
247088-44-4
Molecular Formula
C16H23NO5
Molecular Weight
309.36
MDL Number
MFCD00468832
PubChem ID
4395475
Conditions
Store at 0-8°C
General Information
CAS Number
247088-44-4
Molecular Formula
C16H23NO5
Molecular Weight
309.36
MDL Number
MFCD00468832
PubChem ID
4395475
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

N-(Tert-Butoxycarbonyl)-O-Ethyltyrosine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions without unwanted side reactions. Its stability under various conditions makes it a preferred choice for chemists.
  • Drug Development: In pharmaceutical research, it is used to modify amino acids, enhancing the bioavailability and efficacy of drug candidates. This modification can lead to improved therapeutic profiles.
  • Bioconjugation: The compound facilitates the attachment of biomolecules to surfaces or other molecules, which is crucial in developing targeted drug delivery systems and diagnostic tools.
  • Research in Neuroscience: It is employed in studies involving neurotransmitter pathways, particularly in the development of compounds that can modulate receptor activity, offering insights into neurological disorders.
  • Analytical Chemistry: The compound is utilized in various analytical techniques, including chromatography, to separate and identify complex mixtures, aiding researchers in characterizing new substances.

Citations