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Catalog Number:
47713
CAS Number:
2389078-71-9
Na-(4,4-Dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-Nb-Fmoc-L-2,3-diaminopropionic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
ivDde-Dap(Fmoc)-OH
Antibiotic
Documents
$70.00 /25MG
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Product Information

Na-(4,4-Dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-Nb-Fmoc-L-2,3-diaminopropionic acid is a specialized compound that serves as a valuable building block in peptide synthesis and drug development. This compound is particularly notable for its unique structural features, which enhance its stability and reactivity, making it an ideal candidate for researchers focused on developing novel therapeutic agents. Its Fmoc (9-fluorenylmethoxycarbonyl) protective group allows for easy incorporation into peptide chains, facilitating the synthesis of complex biomolecules with precision.

In practical applications, this compound is utilized in the design of peptide-based drugs, where its ability to form stable linkages is crucial. Additionally, its unique cyclohexenone structure provides opportunities for further functionalization, enabling the development of compounds with tailored biological activities. Researchers in medicinal chemistry and biochemistry will find this compound particularly beneficial for advancing their projects, as it combines versatility with robust performance in various synthetic pathways.

Synonyms
ivDde-Dap(Fmoc)-OH
CAS Number
2389078-71-9
Purity
≥ 99% (HPLC)
Molecular Formula
C31H36N2O6
Molecular Weight
532.6
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -57 to -53 ° (C=1 in MeOH)
Conditions
Store at 2 - 8 °C
General Information
Synonyms
ivDde-Dap(Fmoc)-OH
CAS Number
2389078-71-9
Purity
≥ 99% (HPLC)
Molecular Formula
C31H36N2O6
Molecular Weight
532.6
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -57 to -53 ° (C=1 in MeOH)
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
Yes
DEA-regulated
No
Warnings
-
Applications

Na-(4,4-Dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-Nb-Fmoc-L-2,3-diaminopropionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, which are crucial for developing new drugs and therapeutic agents.
  • Drug Development: Its unique structure allows for the creation of novel pharmaceutical compounds, enhancing efficacy and reducing side effects in treatments.
  • Bioconjugation: The compound can be used to attach biomolecules to surfaces or other molecules, facilitating targeted drug delivery systems in cancer therapy.
  • Research in Neuroscience: It plays a role in studying neuropeptides, contributing to the understanding of neurological disorders and potential treatments.
  • Material Science: The chemical's properties can be exploited in creating advanced materials, such as hydrogels, which have applications in tissue engineering and regenerative medicine.

Citations