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Catalog Number:
03765
CAS Number:
608512-86-3
Ester γ-9-fluorénylméthylique de l'acide Fmoc-L-glutamique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Glu(OFm)-OH, Ester 5-(9-fluorénylméthyl) de l'acide Fmoc-L-glutamique
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Product Information

Fmoc-L-glutamic acid g-9-fluorenylmethyl ester is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound serves as a protective group for the amino functionality of glutamic acid, facilitating the formation of peptide bonds while preventing unwanted side reactions. Its unique structure, featuring the fluorenylmethyl ester, enhances solubility and stability, making it an ideal choice for researchers engaged in solid-phase peptide synthesis and other organic synthesis applications.

In addition to its role in peptide synthesis, Fmoc-L-glutamic acid g-9-fluorenylmethyl ester is also valuable in the development of pharmaceutical compounds, particularly in the design of peptide-based therapeutics. Its ability to provide a stable and easily removable protecting group allows for the efficient assembly of complex peptide sequences, which is crucial in the production of biologically active molecules. This compound is essential for researchers looking to streamline their synthesis processes while ensuring high yields and purity in their final products.

Synonyms
Fmoc-L-Glu(OFm)-OH, Ester 5-(9-fluorénylméthyl) de l'acide Fmoc-L-glutamique
CAS Number
608512-86-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C 34 H 296
Molecular Weight
547.6
MDL Number
MFCD01631978
PubChem ID
76401351
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = 4 ± 2° (C=1 dans l'acétate d'éthyle)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-L-Glu(OFm)-OH, Ester 5-(9-fluorénylméthyl) de l'acide Fmoc-L-glutamique
CAS Number
608512-86-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C 34 H 296
Molecular Weight
547.6
MDL Number
MFCD01631978
PubChem ID
76401351
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = 4 ± 2° (C=1 dans l'acétate d'éthyle)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

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

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups. Its stability under various conditions makes it a preferred choice for chemists.
  • Drug Development: In pharmaceutical research, it plays a role in the design and synthesis of bioactive peptides, which can lead to the development of new therapeutics targeting specific diseases.
  • Bioconjugation: The compound is used in bioconjugation techniques, enabling the attachment of peptides to other biomolecules or surfaces, which is crucial for creating targeted drug delivery systems.
  • Protein Engineering: Researchers utilize it in the modification of proteins, enhancing their stability and functionality, which is essential in fields like biotechnology and enzyme engineering.
  • Analytical Chemistry: It aids in the development of analytical methods for peptide characterization, providing insights into peptide structure and function, which is vital for quality control in peptide-based products.

Citations