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Catalog Number:
03695
CAS Number:
269066-08-2
Fmoc-L-aspartic acid ॆ-4-[N-{1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl}amino]benzyl ester
Purity:
≥ 99.5% (Chiral HPLC)
Synonym(s):
Fmoc-L-Asp(ODmab)-OH
Documents
$72.31 /100MG
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Product Information

Fmoc-L-aspartic acid b-4-[N-{1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl}amino]benzyl ester is a specialized amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its structure allows for the incorporation of complex side chains, making it particularly valuable in the design of bioactive peptides and pharmaceuticals. Researchers in the fields of medicinal chemistry and biochemistry can leverage this compound to create tailored peptides that exhibit enhanced biological activity and specificity.

The compound's distinctive properties, such as its stability and compatibility with various coupling reagents, facilitate efficient peptide synthesis, enabling the development of novel therapeutics. Its application extends to the creation of peptide-based drugs, which are increasingly important in treating a range of diseases, including cancer and metabolic disorders. By utilizing Fmoc-L-aspartic acid b-4-[N-{1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl}amino]benzyl ester, researchers can streamline their synthesis processes while achieving high yields and purity, making it an essential tool in modern pharmaceutical research.

Synonyms
Fmoc-L-Asp(ODmab)-OH
CAS Number
269066-08-2
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C39H42N2O8
Molecular Weight
666.7
MDL Number
MFCD00797875
PubChem ID
137295287
Melting Point
142 - 147 °C
Appearance
White to yellow powder or off-white powder
Optical Rotation
[a]D25 = 25 ± 2.5 º (C=1 in CH2Cl2
Conditions
Store at ≤ -15 °C
General Information
Synonyms
Fmoc-L-Asp(ODmab)-OH
CAS Number
269066-08-2
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C39H42N2O8
Molecular Weight
666.7
MDL Number
MFCD00797875
PubChem ID
137295287
Melting Point
142 - 147 °C
Appearance
White to yellow powder or off-white powder
Optical Rotation
[a]D25 = 25 ± 2.5 º (C=1 in CH2Cl2
Conditions
Store at ≤ -15 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-L-aspartic acid b-4-[N-{1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl}amino]benzyl es is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, facilitating the incorporation of aspartic acid into peptide chains, which is crucial for developing various therapeutic proteins.
  • Drug Development: Its unique structure allows researchers to modify drug candidates, enhancing their efficacy and specificity, particularly in designing inhibitors for specific biological targets.
  • Bioconjugation: The compound is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, improving the delivery and effectiveness of drugs in targeted therapies.
  • Research in Neuroscience: Due to its role in neurotransmitter function, it is valuable in studies investigating neurological disorders, helping to develop potential treatments.
  • Material Science: The compound can be utilized in creating advanced materials with specific properties, such as biocompatibility and enhanced mechanical strength, for applications in medical devices.

Citations