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Catalog Number:
05536
CAS Number:
133906-29-3
Boc-L-glutamic acid ॅ-9-fluorenylmethyl ester
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-L-Glu-OFm
Documents
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Product Information

Boc-L-glutamic acid a-9-fluorenylmethyl ester is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This protected amino acid derivative features a Boc (tert-butoxycarbonyl) group that enhances its stability and solubility, making it an ideal choice for various applications in organic synthesis. Its unique structure, characterized by the fluorenylmethyl ester, allows for selective deprotection under mild conditions, facilitating the formation of complex peptides and proteins. Researchers often leverage this compound in the development of novel therapeutics, particularly in the fields of drug discovery and biochemistry, where precise amino acid sequences are crucial.

The compound's ability to serve as a building block in the synthesis of bioactive peptides underscores its importance in medicinal chemistry. Additionally, its favorable properties, such as high purity and excellent yield, make it a preferred choice for professionals seeking reliable reagents for their research. With its significant role in advancing peptide-based therapies, Boc-L-glutamic acid a-9-fluorenylmethyl ester stands out as a key component in the toolkit of researchers and industry professionals alike.

Synonyms
Boc-L-Glu-OFm
CAS Number
133906-29-3
Purity
≥ 99% (HPLC)
Molecular Formula
C24H27NO6
Molecular Weight
425.48
MDL Number
MFCD00151872
PubChem ID
4712640
Appearance
White powder
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-L-Glu-OFm
CAS Number
133906-29-3
Purity
≥ 99% (HPLC)
Molecular Formula
C24H27NO6
Molecular Weight
425.48
MDL Number
MFCD00151872
PubChem ID
4712640
Appearance
White powder
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

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

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups. This is crucial in developing complex peptides for pharmaceuticals.
  • Drug Development: Its application in medicinal chemistry helps in designing and optimizing drug candidates, particularly those targeting neurological disorders, by modifying amino acid sequences for improved efficacy.
  • Bioconjugation: The compound is used in bioconjugation processes, linking biomolecules such as proteins and antibodies to therapeutic agents, enhancing their delivery and effectiveness in targeted therapies.
  • Research in Protein Engineering: It aids in the modification of proteins, allowing researchers to study structure-function relationships, which is essential for developing new biocatalysts or therapeutic proteins.
  • Analytical Chemistry: The compound is utilized in various analytical techniques, such as HPLC, to separate and identify amino acids and peptides, providing valuable insights into biochemical processes.

Citations