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Catalog Number:
29637
CAS Number:
685863-48-3
Acide R -Fmoc-2-amino-3-(2- tert -butoxycarbonyl-éthylsulfanyl)-propionique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Cys( tert -butoxycarbonyléthyl)-OH
Documents
$106.96 /100 mg
Taille
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Informations sur le produit

(R)-Fmoc-2-amino-3-(2-tert-butoxycarbonyl-ethylsulfanyl)-propionic acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure, incorporating a tert-butoxycarbonyl group and a sulfanyl moiety, enhances its stability and solubility, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry.

This compound is particularly valuable in the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its application extends to the synthesis of complex peptides that can be used in various biological assays, drug discovery, and the development of novel therapeutic agents. The ability to easily manipulate its structure allows for the exploration of diverse chemical properties, making it a preferred choice for professionals seeking reliable and efficient solutions in peptide synthesis.

Numéro CAS 
685863-48-3
Formule moléculaire
C 25 H 29 NON 6 S
Poids moléculaire 
471.57
Rotation optique 
[a] D 20 = -28,3 ± 2º (C = 1 dans DMF)
Informations générales
Numéro CAS 
685863-48-3
Formule moléculaire
C 25 H 29 NON 6 S
Poids moléculaire 
471.57
Rotation optique 
[a] D 20 = -28,3 ± 2º (C = 1 dans DMF)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

(R)-Fmoc-2-amino-3-(2-tert-butoxycarbonyl-ethylsulfanyl)-propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), allowing for the creation of complex peptide sequences with high purity.
  • Drug Development: It plays a crucial role in the pharmaceutical industry for developing peptide-based drugs, offering a pathway to create therapeutics with enhanced efficacy and specificity.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of peptides to other biomolecules, which is essential for creating targeted drug delivery systems.
  • Research in Protein Engineering: It aids researchers in modifying proteins to study their functions and interactions, contributing to advancements in biotechnology and molecular biology.
  • Diagnostic Applications: The compound can be utilized in the development of diagnostic tools, particularly in assays that require specific peptide interactions, enhancing the sensitivity and accuracy of tests.

Citations