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Catalog Number:
07104
CAS Number:
872169-32-9
Nα-Fmoc-Nγ-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-D-2,4-diaminobutyric acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-D-Dab(ivDde)-OH
Documents
$72.31 /100MG
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Product Information

Na-Fmoc-Ng-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-D-2,4-diaminobutyric acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound features the Fmoc (9-fluorenylmethoxycarbonyl) protective group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique structure, incorporating a cyclohexenone moiety, enhances its reactivity and stability, making it an ideal candidate for researchers focused on developing novel therapeutic agents.

In the pharmaceutical industry, this compound can be employed in the design of peptide-based drugs, particularly those targeting specific biological pathways. Its ability to facilitate the formation of complex structures allows for the exploration of new drug candidates with improved efficacy and reduced side effects. Additionally, its application in combinatorial chemistry can lead to the rapid generation of diverse libraries of compounds, accelerating the drug discovery process. Researchers will find this compound invaluable for its efficiency and effectiveness in advancing their projects.

Synonyms
Fmoc-D-Dab(ivDde)-OH
CAS Number
872169-32-9
Purity
≥ 99% (HPLC)
Molecular Formula
C32H38N2O6
Molecular Weight
546.3
MDL Number
MFCD01631665
PubChem ID
137238785
Melting Point
127 - 138 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = 13 ± 2 º (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-D-Dab(ivDde)-OH
CAS Number
872169-32-9
Purity
≥ 99% (HPLC)
Molecular Formula
C32H38N2O6
Molecular Weight
546.3
MDL Number
MFCD01631665
PubChem ID
137238785
Melting Point
127 - 138 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = 13 ± 2 º (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Fmoc-Ng-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-D-2,4-diaminobutyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting the overall structure. This is crucial for developing complex peptides in pharmaceutical research.
  • Drug Development: Its unique structure aids in the design of novel drug candidates, particularly in targeting specific biological pathways. Researchers can leverage its properties to create more effective therapeutic agents.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules to other entities like drugs or imaging agents. This enhances the delivery and efficacy of therapeutic compounds in targeted therapies.
  • Research in Cancer Therapeutics: Due to its ability to interact with specific cellular targets, it is being explored in the development of cancer treatments, providing a pathway for more personalized medicine approaches.
  • Material Science: It can also be utilized in the development of advanced materials, particularly in creating functionalized surfaces that can be used in sensors or drug delivery systems, showcasing its versatility beyond traditional applications.

Citations