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Catalog Number:
16149
CAS Number:
1263045-85-7
Acide N α -(4,4-diméthyl-2,6-dioxocyclohex-1-ylidène)éthyl- N γ -Fmoc-L-2,4-diaminobutyrique
Purity:
≥ 99 % (HPLC, CCM)
Synonym(s):
Dde-L-Dab(Fmoc)-OH
Documents
$82.02 /100 mg
Taille
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Product Information

Na-(4,4-Dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl-Ng-Fmoc-L-2,4-diaminobutyric acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique structure that enhances its stability and bioavailability, making it an excellent choice for researchers focused on developing novel therapeutics. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy incorporation into peptide chains, facilitating the synthesis of complex biomolecules.

In the pharmaceutical industry, this compound can be employed in the design of peptide-based drugs, particularly those targeting specific receptors or pathways. Its distinctive cyclohexenone moiety contributes to its reactivity, enabling the formation of diverse chemical derivatives that can be tailored for specific applications. Researchers appreciate its potential for improving the efficacy and selectivity of therapeutic agents, making it a valuable addition to any laboratory focused on innovative drug design.

Synonyms
Dde-L-Dab(Fmoc)-OH
CAS Number
1263045-85-7
Purity
≥ 99 % (HPLC, CCM)
Molecular Formula
C29H32N2O6
Molecular Weight
504.6
MDL Number
MFCD05663743
PubChem ID
137704931
Melting Point
148 - 156 °C
Appearance
Poudre cristalline blanche
Optical Rotation
[a] D 20 = -38 ± 1 º (C = 1 dans MeOH)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Dde-L-Dab(Fmoc)-OH
CAS Number
1263045-85-7
Purity
≥ 99 % (HPLC, CCM)
Molecular Formula
C29H32N2O6
Molecular Weight
504.6
MDL Number
MFCD05663743
PubChem ID
137704931
Melting Point
148 - 156 °C
Appearance
Poudre cristalline blanche
Optical Rotation
[a] D 20 = -38 ± 1 º (C = 1 dans MeOH)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Na-(4,4-Dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl-Ng-Fmoc-L-2,4-diaminobutyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, which are essential for developing new drugs and therapeutic agents.
  • Drug Development: Its unique structure allows researchers to create novel compounds with potential pharmaceutical applications, particularly in targeting specific biological pathways.
  • Bioconjugation: It is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, enhancing the efficacy of drug delivery systems.
  • Research in Cancer Therapeutics: The compound's properties make it a candidate for studies aimed at developing targeted cancer therapies, potentially improving treatment outcomes.
  • Analytical Chemistry: It can be employed in analytical methods to study interactions between biomolecules, aiding in the understanding of complex biological systems.

Citations