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Catalog Number:
37076
CAS Number:
2308529-94-2
N α - (4,4-diméthyl-2,6-dioxocyclohex-1-ylidène)-3-méthylbutyl- N ε -Fmoc-D-lysine
Purity:
≥ 99 % (HPLC, CCM)
Synonym(s):
ivDde-D-Lys(Fmoc)-OH
Documents
$72.31 /100 mg
Taille
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Informations sur le produit

Na - (4,4-Dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl- Ne -Fmoc-D-lysine is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which facilitates the selective modification of peptides, making it an essential tool for researchers in the fields of biochemistry and medicinal chemistry. Its structural properties, including the 4,4-dimethyl-2,6-dioxocyclohex-1-ylidene moiety, enhance its stability and reactivity, allowing for efficient coupling reactions in solid-phase peptide synthesis.

This compound is particularly beneficial for the synthesis of complex peptides and proteins, enabling the development of novel therapeutics and biologically active molecules. Its ability to provide high yields and purity in peptide synthesis makes it a preferred choice among professionals. Additionally, the unique structural features of Na - (4,4-Dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl- Ne -Fmoc-D-lysine allow for improved solubility and bioavailability, which are critical factors in drug formulation and delivery.

Numéro CAS 
2308529-94-2
Formule moléculaire
C34H42N2O6
Poids moléculaire 
574.7
Point de fusion 
79 - 84 °C
Rotation optique 
[a] 20 D = -11 ± 2 º (C = 1 dans CHCl 3 )
Informations générales
Numéro CAS 
2308529-94-2
Formule moléculaire
C34H42N2O6
Poids moléculaire 
574.7
Point de fusion 
79 - 84 °C
Rotation optique 
[a] 20 D = -11 ± 2 º (C = 1 dans CHCl 3 )
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

Na - (4,4-Dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl- Ne -Fmoc-D-lysine 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, enhancing the efficiency and yield of desired products.
  • Drug Development: Its unique structure allows for the design of novel pharmaceutical agents, particularly in the field of cancer research, where modifications can lead to improved efficacy and reduced side effects.
  • Bioconjugation: The chemical is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial in the development of targeted therapies and diagnostics.
  • Research in Protein Engineering: It aids in the modification of lysine residues in proteins, facilitating studies on protein structure and function, which is essential for understanding biological mechanisms.
  • Material Science: The compound can be incorporated into polymer systems to enhance material properties, such as thermal stability and mechanical strength, making it valuable in the development of advanced materials.

Citations