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Catalog Number:
03705
CAS Number:
172611-75-5
Fmoc-L-glutamic acid-a-4-[N-{1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl}amino] benzyl ester
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-Glu-ODmab
Documents
$65.40 /100MG
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Product Information

Fmoc-L-glutamic acid-a-4-[N-{1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl}amino] benzyl e 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 solid-phase peptide synthesis. Its unique structure allows for enhanced stability and reactivity, making it an ideal choice for researchers focused on developing complex peptides and biologically active compounds.

In addition to its role in peptide synthesis, this compound is also valuable in medicinal chemistry, particularly in the design of novel therapeutics. Its ability to facilitate the incorporation of specific functional groups into peptide chains opens up possibilities for creating targeted drug delivery systems and improving the efficacy of therapeutic agents. Researchers in the fields of biochemistry and pharmaceutical development will find this compound particularly beneficial for its versatility and the potential to streamline the synthesis of intricate peptide structures.

Synonyms
Fmoc-L-Glu-ODmab
CAS Number
172611-75-5
Purity
≥ 98% (HPLC)
Molecular Formula
C40H44N2O8
Molecular Weight
680.8
MDL Number
MFCD00797874
PubChem ID
137295288
Melting Point
73 - 80 °C
Appearance
Off-white to yellowish orange solid
Optical Rotation
[a]25D = - 19 ± 1 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-Glu-ODmab
CAS Number
172611-75-5
Purity
≥ 98% (HPLC)
Molecular Formula
C40H44N2O8
Molecular Weight
680.8
MDL Number
MFCD00797874
PubChem ID
137295288
Melting Point
73 - 80 °C
Appearance
Off-white to yellowish orange solid
Optical Rotation
[a]25D = - 19 ± 1 º (C=1 in DMF)
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

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

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing for the selective modification of amino acids without affecting the overall structure. This is crucial in developing complex peptides for pharmaceuticals.
  • Drug Development: Its unique structure aids in the design of novel drug candidates, particularly in targeting specific biological pathways. This can lead to more effective treatments with fewer side effects.
  • Bioconjugation: The compound is used to create bioconjugates, which are essential in developing targeted therapies and diagnostic tools in the biomedical field, enhancing the precision of treatments.
  • Research in Neuroscience: Its applications extend to neuroscience research, where it helps in studying neurotransmitter pathways, providing insights into neurological disorders and potential therapies.
  • Material Science: The compound is also explored in material science for creating functionalized polymers, which can be used in various applications, including drug delivery systems and biosensors.

Citations