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Catalog Number:
03182
CAS Number:
198543-46-3
Fmoc- S -acétamidométhyl-L-cystéinol
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Cystéinol (Acm), Fmoc-L-Cys(Acm)-ol
Documents
$132.20 /1G
Taille
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Informations sur le produit

Fmoc-S-acetamidomethyl-L-cysteinol is a versatile compound widely utilized in peptide synthesis and drug development. This protected amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) group, which provides stability during the synthesis process while allowing for easy deprotection. Its unique structure, characterized by the acetamidomethyl and hydroxyl functionalities, enhances its reactivity and compatibility with various coupling agents, making it an excellent choice for researchers focused on creating complex peptides and proteins.

In addition to its role in peptide synthesis, Fmoc-S-acetamidomethyl-L-cysteinol is particularly valuable in the development of therapeutics targeting cysteine-rich proteins, which are crucial in many biological processes. Its application extends to the fields of medicinal chemistry and biochemistry, where it aids in the design of inhibitors and modulators for various biological pathways. Researchers appreciate its ability to streamline synthesis while maintaining high purity and yield, making it a preferred choice in both academic and industrial laboratories.

Numéro CAS 
198543-46-3
Formule moléculaire
C21H24N2O4S
Poids moléculaire 
400.5
Point de fusion 
135 - 137 °C
Rotation optique 
[a] 20 D = -31 ± 2 ° (C=1 dans MeOH)
Informations générales
Numéro CAS 
198543-46-3
Formule moléculaire
C21H24N2O4S
Poids moléculaire 
400.5
Point de fusion 
135 - 137 °C
Rotation optique 
[a] 20 D = -31 ± 2 ° (C=1 dans MeOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
-
Applications

Fmoc-S-acetamidomethyl-L-cysteinol 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 plays a crucial role in the design of novel pharmaceuticals, particularly in creating compounds that target specific biological pathways.
  • Bioconjugation: Researchers use it to attach biomolecules, such as proteins or antibodies, to other molecules, enhancing the efficacy of therapeutic agents.
  • Analytical Chemistry: The compound is employed in various analytical techniques, aiding in the identification and quantification of complex mixtures.
  • Biotechnology: It is essential in the development of biosensors and other biotechnological applications, improving sensitivity and specificity in detection methods.

Citations