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Catalog Number:
14440
CAS Number:
232953-09-2
Fmoc- S -allyloxycarbonylamidométhyl-L-cystéine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Cys(Allocam)-OH
Documents
$132.80 /100 mg
Taille
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Informations sur le produit

Fmoc-S-allyloxycarbonylamidomethyl-L-cysteine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethyloxycarbonyl) protecting group, which facilitates the selective protection of the amino group during the synthesis of complex peptides. Its allyloxycarbonyl moiety enhances its reactivity and compatibility in various coupling reactions, making it an excellent choice for researchers focused on synthesizing bioactive peptides and pharmaceuticals.

The compound's structure allows for easy incorporation into peptide chains, providing researchers with the ability to create tailored peptides for therapeutic applications, including cancer treatment and drug delivery systems. Its stability and reactivity under standard laboratory conditions make it a reliable choice for both academic and industrial applications. With its unique properties, Fmoc-S-allyloxycarbonylamidomethyl-L-cysteine stands out as a valuable tool for chemists and biochemists aiming to innovate in the field of peptide chemistry.

Numéro CAS 
232953-09-2
Formule moléculaire
C23H24N2O6S
Poids moléculaire 
456.51
Rotation optique 
[a] D 20 = -32 ± 2 º (C = 1 dans MeOH)
Informations générales
Numéro CAS 
232953-09-2
Formule moléculaire
C23H24N2O6S
Poids moléculaire 
456.51
Rotation optique 
[a] D 20 = -32 ± 2 º (C = 1 dans MeOH)
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

Fmoc-S-allyloxycarbonylamidomethyl-L-cysteine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing for the incorporation of specific functionalities that enhance biological activity.
  • Drug Development: It plays a crucial role in the development of novel therapeutics, particularly in designing drugs that target specific proteins or enzymes in disease pathways.
  • Bioconjugation: The compound is used in bioconjugation techniques, enabling the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Research in Cancer Therapeutics: Its unique structure allows researchers to explore new avenues in cancer treatment by modifying the compound to improve selectivity and efficacy against cancer cells.
  • Protein Engineering: The compound is beneficial in protein engineering applications, where it aids in the design of proteins with enhanced stability and functionality for various industrial and therapeutic uses.

Citations