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Catalog Number:
03706
CAS Number:
268730-86-5
Fmoc-L-glutamic acid े-4-[N-{1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl}amino] benzyl ester
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-Glu(ODmab)-OH
Documents
$55.48 /100MG
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Product Information

Fmoc-L-glutamic acid g-4-[N-{1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl}amino] benzyl e is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which is crucial for the selective protection of amino acids during the synthesis of peptides. Its unique structure allows for the introduction of complex side chains, making it an invaluable tool for researchers working on the design of novel peptides and therapeutic agents.

In the pharmaceutical industry, this compound can be employed in the development of targeted drug delivery systems and in the synthesis of biologically active peptides. Its ability to facilitate the incorporation of diverse functional groups enhances its applicability in medicinal chemistry, particularly in the creation of compounds with improved bioactivity and specificity. Researchers appreciate its stability and ease of use, which streamline the peptide synthesis process, ultimately leading to more efficient development timelines for new therapeutics.

Synonyms
Fmoc-L-Glu(ODmab)-OH
CAS Number
268730-86-5
Purity
≥ 98% (HPLC)
Molecular Formula
C40H44N2O8
Molecular Weight
680.8
MDL Number
MFCD00797873
PubChem ID
137795621
Melting Point
160 - 180 °C
Appearance
Light yellow or off-white powder
Optical Rotation
[a]D20 = -1.0 to -2.5 º (C=4 in DMF)
Conditions
Store at ≤ -4 °C
General Information
Synonyms
Fmoc-L-Glu(ODmab)-OH
CAS Number
268730-86-5
Purity
≥ 98% (HPLC)
Molecular Formula
C40H44N2O8
Molecular Weight
680.8
MDL Number
MFCD00797873
PubChem ID
137795621
Melting Point
160 - 180 °C
Appearance
Light yellow or off-white powder
Optical Rotation
[a]D20 = -1.0 to -2.5 º (C=4 in DMF)
Conditions
Store at ≤ -4 °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 g-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 key building block in the synthesis of peptides, allowing researchers to create complex molecules for drug development and biological studies.
  • Drug Design: Its unique structure aids in the design of novel pharmaceuticals, particularly in targeting specific receptors in the body, enhancing therapeutic efficacy.
  • Bioconjugation: The compound can be used in bioconjugation techniques, linking drugs to antibodies or other biomolecules, which is crucial for targeted therapy in cancer treatment.
  • Research in Neuroscience: It plays a role in studying neurotransmitter functions and developing treatments for neurological disorders by mimicking natural amino acids.
  • Material Science: This chemical is also explored in the development of smart materials, where its properties can be harnessed for creating responsive systems in various applications.

Citations