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Catalog Number:
12863
CAS Number:
30044-61-2
Boc- S - tert -butylthio-L-cystéine
Purity:
≥ 99,5 % (pureté chirale)
Synonym(s):
Boc-L-Cys(StBu)-OH, Boc- S - tert -butylmercapto-L-cystéine
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$70.00 /1G
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Informations sur le produit

Boc-S-tert-butylthio-L-cysteine is a versatile compound widely utilized in the fields of biochemistry and pharmaceutical research. This amino acid derivative features a tert-butyldisulfanyl group, enhancing its stability and reactivity, making it an excellent choice for synthesizing peptide-based therapeutics and drug candidates. Its unique structure allows for selective modifications, facilitating the development of novel compounds with improved bioactivity and pharmacokinetic properties. Researchers often employ Boc-S-tert-butylthio-L-cysteine in the synthesis of complex peptides, where it serves as a valuable building block due to its protective Boc group, which can be easily removed under mild conditions.

In addition to its role in peptide synthesis, Boc-S-tert-butylthio-L-cysteine has shown potential in studies related to oxidative stress and cellular signaling pathways. Its application in drug discovery and development is further supported by its ability to enhance the solubility and stability of various compounds. This makes it a preferred choice for researchers aiming to optimize lead compounds for therapeutic use. Overall, Boc-S-tert-butylthio-L-cysteine stands out for its practical applications in medicinal chemistry and its contribution to advancing research in the pharmaceutical industry.

Numéro CAS 
30044-61-2
Formule moléculaire
C 12 H 23 NON 4 S 2
Poids moléculaire 
309.45
Point de fusion 
116 - 122 °C
Rotation optique 
[a] D 25 = -145 ± 5 º (C=2 dans MeOH)
Informations générales
Numéro CAS 
30044-61-2
Formule moléculaire
C 12 H 23 NON 4 S 2
Poids moléculaire 
309.45
Point de fusion 
116 - 122 °C
Rotation optique 
[a] D 25 = -145 ± 5 º (C=2 dans MeOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
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Applications

Boc-S-tert-butylthio-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 selective reactions without interfering with other functional groups.
  • Drug Development: It is used in the design of novel pharmaceuticals, particularly in creating compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The chemical is valuable in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, improving drug delivery systems.
  • Antioxidant Research: Researchers explore its properties in developing antioxidants, which can protect cells from oxidative stress, relevant in various health applications.
  • Analytical Chemistry: It is employed in analytical methods to study protein interactions and modifications, providing insights into biochemical processes.

Citations