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Catalog Number:
03693
CAS Number:
172611-77-7
Fmoc-L-aspartic acid α-4-[N-{1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl}amino]benzyl ester
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-Asp-ODmab
Documents
$110.00 /250MG
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Product Information

Fmoc-L-aspartic acid a-4-[N-{1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl}amino]benzyl es is a specialized amino acid derivative 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 groups during the synthesis of peptides. Its unique structure allows for enhanced stability and solubility, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry.

In practical applications, this compound is particularly valuable in the synthesis of complex peptides and proteins, facilitating the development of therapeutic agents and biologically active compounds. Its ability to provide a robust protective group while maintaining reactivity makes it a preferred choice among professionals looking to streamline their synthesis processes. Additionally, the incorporation of the dimethyl-2,6-dioxocyclohexylidene moiety enhances its utility in creating diverse molecular architectures, paving the way for innovative drug design and discovery.

Synonyms
Fmoc-L-Asp-ODmab
CAS Number
172611-77-7
Purity
≥ 98% (HPLC)
Molecular Formula
C39H42N2O8
Molecular Weight
666.7
MDL Number
MFCD00797876
PubChem ID
137295289
Appearance
Yellow powder
Optical Rotation
[a]D25 = - 17.0 ± 2° (C=1 in DMF)
Conditions
Store at ≤ -15 °C
General Information
Synonyms
Fmoc-L-Asp-ODmab
CAS Number
172611-77-7
Purity
≥ 98% (HPLC)
Molecular Formula
C39H42N2O8
Molecular Weight
666.7
MDL Number
MFCD00797876
PubChem ID
137295289
Appearance
Yellow powder
Optical Rotation
[a]D25 = - 17.0 ± 2° (C=1 in DMF)
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 a-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, particularly in solid-phase peptide synthesis, allowing for the creation of complex and functional peptides used in drug development.
  • Drug Design: It plays a critical role in the design of novel pharmaceuticals, especially those targeting specific biological pathways, enhancing the efficacy and selectivity of drug candidates.
  • Bioconjugation: The compound is used in bioconjugation processes, linking biomolecules to therapeutic agents, which is essential in developing targeted therapies and diagnostic tools.
  • Research in Neuroscience: It is applied in studies related to neurotransmitter pathways, aiding researchers in understanding the role of aspartic acid derivatives in neurological functions and disorders.
  • Material Science: This chemical is explored in the development of smart materials, where its unique properties can be harnessed for creating responsive systems in various applications, including drug delivery and biosensing.

Citations