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Catalog Number:
03704
CAS Number:
200616-18-8
Fmoc-L-glutamic acid α-9-fluorenylmethyl ester
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-Glu-OFm
Documents
$117.78 /1G
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Product Information

Fmoc-L-glutamic acid a-9-fluorenylmethyl ester is a versatile compound widely utilized in peptide synthesis and drug development. This protected amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) group, which provides stability during the synthesis process while allowing for easy deprotection when needed. Its unique structure enhances solubility and reactivity, making it an ideal choice for researchers focused on developing complex peptides and proteins.

In the pharmaceutical industry, Fmoc-L-glutamic acid a-9-fluorenylmethyl ester plays a crucial role in the synthesis of bioactive peptides, which are essential for various therapeutic applications, including cancer treatment and hormone regulation. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of the amino acid chain makes it a preferred choice among chemists and biochemists. With its reliable performance and efficiency, this compound stands out as a key ingredient in advancing peptide-based research and development.

Synonyms
Fmoc-L-Glu-OFm
CAS Number
200616-18-8
Purity
≥ 98% (HPLC)
Molecular Formula
C34H29NO6
Molecular Weight
547.61
MDL Number
MFCD00237656
PubChem ID
76129959
Melting Point
171-178 °C
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-Glu-OFm
CAS Number
200616-18-8
Purity
≥ 98% (HPLC)
Molecular Formula
C34H29NO6
Molecular Weight
547.61
MDL Number
MFCD00237656
PubChem ID
76129959
Melting Point
171-178 °C
Appearance
White powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-L-glutamic acid a-9-fluorenylmethyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in solid-phase peptide synthesis, allowing researchers to create complex peptides efficiently. Its protective Fmoc group simplifies the deprotection process, enhancing yield and purity.
  • Drug Development: In pharmaceutical research, it is used to develop peptide-based drugs. Its structure allows for modifications that can improve bioavailability and target specificity, making it valuable in medicinal chemistry.
  • Bioconjugation: The compound is employed in bioconjugation techniques, where it can be linked to other biomolecules. This application is crucial in creating targeted therapies and diagnostic agents in the field of biotechnology.
  • Protein Engineering: Researchers utilize it to modify proteins, enhancing their stability and functionality. This is particularly beneficial in developing enzymes with improved catalytic properties for industrial applications.
  • Research in Neuroscience: Its derivatives are studied for their potential role in neurotransmitter modulation, contributing to advancements in understanding neurological disorders and developing therapeutic strategies.

Citations