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Catalog Number:
31698
CAS Number:
864876-95-9
Fmoc-L-Glu(OtBu)-O-CH2-Ph-OCH2-CH2-COOH
Purity:
≥ 99.5% (Chiral HPLC)
Documents
$72.31 /1G
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Product Information

Fmoc-L-Glu(OtBu)-O-CH2-Ph-OCH2-CH2-COOH is a versatile 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, including the t-butyl ester and phenyl ether functionalities, enhances its solubility and stability, making it an ideal choice for researchers working in organic synthesis and medicinal chemistry.

In practical applications, Fmoc-L-Glu(OtBu)-O-CH2-Ph-OCH2-CH2-COOH is particularly valuable in the development of peptide-based therapeutics and in the study of protein interactions. Its ability to facilitate the formation of complex peptide sequences allows for the exploration of novel drug candidates and biomolecules. Researchers appreciate its compatibility with various coupling reagents and its effectiveness in solid-phase peptide synthesis, providing a reliable pathway for the creation of high-purity peptides. This compound stands out for its efficiency and reliability, making it a preferred choice for professionals in the pharmaceutical and biotechnology sectors.

CAS Number
864876-95-9
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C34H37NO9
Molecular Weight
603.67
MDL Number
MFCD08457846
PubChem ID
155892833
Appearance
White powder
Optical Rotation
[a]20D = -11 ± 2 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
CAS Number
864876-95-9
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C34H37NO9
Molecular Weight
603.67
MDL Number
MFCD08457846
PubChem ID
155892833
Appearance
White powder
Optical Rotation
[a]20D = -11 ± 2 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-Glu(OtBu)-O-CH2-Ph-OCH2-CH2-COOH 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 researchers to create complex peptide sequences efficiently.
  • Drug Development: It is used in the design of peptide-based therapeutics, providing a framework for the development of new drugs that target specific biological pathways, enhancing efficacy and specificity.
  • Bioconjugation: The chemical's reactive groups facilitate bioconjugation processes, which are essential in creating targeted drug delivery systems and diagnostic agents in the pharmaceutical industry.
  • Research in Neuroscience: This compound is instrumental in studying neurotransmitter functions and developing neuroprotective agents, contributing to advancements in treatments for neurological disorders.
  • Protein Engineering: It aids in the modification of proteins to enhance their stability and activity, which is crucial for applications in biotechnology and enzyme development.

Citations