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Catalog Number:
03702
CAS Number:
247127-51-1
Acide N α -Fmoc- N β -1-(4,4-diméthyl-2,6-dioxocyclohex-1-ylidène)éthyl-L-2,3-diaminopropionique
Purity:
98 - 101 % (dosage par titrage)
Synonym(s):
Fmoc-L-Dap(Dde)-OH
Documents
$93.14 /250 mg
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Product Information

Na-Fmoc-Nb-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl-L-2,3-diaminopropionic acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino acids during solid-phase peptide synthesis. Its unique structural attributes, including the 4,4-dimethyl-2,6-dioxocyclohexenylidene moiety, enhance its stability and reactivity, making it an excellent choice for researchers focused on developing complex peptides and biologically active compounds.

In addition to its applications in synthetic chemistry, this compound is also valuable in the field of medicinal chemistry, where it can be employed in the design of novel therapeutics. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups allows for the creation of diverse peptide libraries. Researchers can leverage this compound to explore new drug candidates, optimize lead compounds, and investigate structure-activity relationships, ultimately contributing to advancements in pharmaceutical development.

Synonyms
Fmoc-L-Dap(Dde)-OH
CAS Number
247127-51-1
Purity
98 - 101 % (dosage par titrage)
Molecular Formula
C28H30N2O6
Molecular Weight
490.5
MDL Number
MFCD01631974
PubChem ID
137317222
Melting Point
175 - 188 ºC
Appearance
Poudre cristalline blanche à blanc cassé
Optical Rotation
[a] D 20 = 4,4 - 7,5 º (C = 1 dans MeOH)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-L-Dap(Dde)-OH
CAS Number
247127-51-1
Purity
98 - 101 % (dosage par titrage)
Molecular Formula
C28H30N2O6
Molecular Weight
490.5
MDL Number
MFCD01631974
PubChem ID
137317222
Melting Point
175 - 188 ºC
Appearance
Poudre cristalline blanche à blanc cassé
Optical Rotation
[a] D 20 = 4,4 - 7,5 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-Fmoc-Nb-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl-L-2,3-diaminopropionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting the overall structure. This is crucial for researchers developing new therapeutic peptides.
  • Drug Development: Its unique structure can be leveraged to create novel drug candidates, particularly in the field of targeted therapies, enhancing the efficacy and specificity of treatments.
  • Bioconjugation: The compound can be used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, improving the performance of diagnostic tools and drug delivery systems.
  • Material Science: It finds applications in the development of advanced materials, particularly those requiring specific chemical functionalities, which can lead to innovations in coatings and polymers.
  • Research in Medicinal Chemistry: The compound is valuable in medicinal chemistry for studying structure-activity relationships (SAR), aiding researchers in understanding how modifications affect biological activity.

Citations