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Catalog Number:
05469
CAS Number:
85003-76-5
Boc-S-Z-aminoethyl-L-cysteine
Purity:
≥ 99% (TLC)
Synonym(s):
Boc-L-Cys(Z-NHEt)-OH
Documents
$127.79 /250MG
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Product Information

Boc-S-Z-aminoethyl-L-cysteine is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This amino acid derivative features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and reactivity during chemical reactions. Its unique structure allows for the selective introduction of sulfur-containing functionalities, making it an essential building block in the development of bioactive peptides and therapeutic agents. Researchers appreciate its ability to facilitate the formation of disulfide bonds, which are crucial for the stability and functionality of many proteins.

In addition to its applications in peptide synthesis, Boc-S-Z-aminoethyl-L-cysteine has shown potential in drug design and development, particularly in the creation of targeted therapies for various diseases. Its compatibility with standard coupling reagents and ease of handling make it a preferred choice for chemists looking to streamline their synthesis processes. With its unique properties and practical applications, Boc-S-Z-aminoethyl-L-cysteine stands out as a valuable tool for researchers and industry professionals alike.

Synonyms
Boc-L-Cys(Z-NHEt)-OH
CAS Number
85003-76-5
Purity
≥ 99% (TLC)
Molecular Formula
C18H26N2O6S
Molecular Weight
398.48
MDL Number
MFCD00236840
PubChem ID
13531520
Appearance
Clear, colorless oil
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-L-Cys(Z-NHEt)-OH
CAS Number
85003-76-5
Purity
≥ 99% (TLC)
Molecular Formula
C18H26N2O6S
Molecular Weight
398.48
MDL Number
MFCD00236840
PubChem ID
13531520
Appearance
Clear, colorless oil
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

Boc-S-Z-aminoethyl-L-cysteine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting others. This is crucial in developing complex peptides for pharmaceuticals.
  • Drug Development: Its unique structure aids in the design of novel drugs, particularly those targeting cysteine residues in proteins, which are often involved in various diseases, including cancer and neurodegenerative disorders.
  • Bioconjugation: The compound is used in bioconjugation techniques, where it helps attach biomolecules to surfaces or other molecules, enhancing the efficacy of therapeutic agents and diagnostic tools.
  • Research in Redox Biology: It plays a role in studying redox reactions in biological systems, providing insights into oxidative stress and its implications in health and disease.
  • Antioxidant Studies: Researchers utilize this compound to investigate its potential antioxidant properties, contributing to the development of supplements or drugs aimed at reducing oxidative damage in cells.

Citations