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Catalog Number:
11190
CAS Number:
141743-15-9
Fmoc-N-(2-Boc-aminoethyl)glycine
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-N-(N-β-Boc-aminoethyl)-Gly-OH, Fmoc-Aeg(Boc)-OH
Hazmat
Documents
$93.14 /100MG
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Product Information

Fmoc-N-(2-Boc-aminoethyl)glycine is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which facilitates the selective deprotection of amino acids during solid-phase peptide synthesis. Its Boc (tert-butyloxycarbonyl) group enhances stability and solubility, making it an ideal choice for researchers focused on synthesizing complex peptides and biologically active compounds.

In practical applications, Fmoc-N-(2-Boc-aminoethyl)glycine serves as a crucial intermediate in the preparation of peptide-based therapeutics, particularly in the fields of medicinal chemistry and biochemistry. Its unique structure allows for the incorporation of diverse functional groups, enabling the design of peptides with tailored properties for specific biological activities. Researchers can leverage this compound to streamline their synthesis processes, improve yields, and enhance the overall efficiency of their projects.

Synonyms
Fmoc-N-(N-β-Boc-aminoethyl)-Gly-OH, Fmoc-Aeg(Boc)-OH
CAS Number
141743-15-9
Purity
≥ 99% (HPLC)
Molecular Formula
C24H28N2O6
Molecular Weight
440.5
MDL Number
MFCD02259490
PubChem ID
2756167
Appearance
White crystalline powder
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-N-(N-β-Boc-aminoethyl)-Gly-OH, Fmoc-Aeg(Boc)-OH
CAS Number
141743-15-9
Purity
≥ 99% (HPLC)
Molecular Formula
C24H28N2O6
Molecular Weight
440.5
MDL Number
MFCD02259490
PubChem ID
2756167
Appearance
White crystalline powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-N-(2-Boc-aminoethyl)glycine 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 structures with high specificity and efficiency.
  • Drug Development: It is used in the pharmaceutical industry for developing new drugs, particularly in designing peptide-based therapeutics that can target specific biological pathways.
  • Bioconjugation: The chemical is valuable in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial for creating targeted drug delivery systems.
  • Research in Biochemistry: It aids in studying protein interactions and functions, providing insights into cellular mechanisms and potential therapeutic targets.
  • Custom Synthesis: Researchers often utilize it for custom synthesis projects, allowing for tailored modifications in peptide sequences that can enhance stability and bioactivity.

Citations