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Catalog Number:
15067
CAS Number:
174799-89-4
Fmoc-N-(tert-butyloxycarbonylethyl)glycine
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-Nglu(OtBu)-OH
Documents
$58.39 /100MG
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Product Information

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

In the pharmaceutical industry, Fmoc-N-(tert-butyloxycarbonylethyl)glycine serves as a crucial building block for the development of peptide-based therapeutics, including those targeting cancer and metabolic disorders. Its unique structure allows for the incorporation of various functional groups, enabling the design of tailored peptides with enhanced efficacy and specificity. Researchers appreciate its ease of use and compatibility with standard coupling reagents, making it a preferred choice in both academic and industrial settings.

Synonyms
Fmoc-Nglu(OtBu)-OH
CAS Number
174799-89-4
Purity
≥ 99% (HPLC)
Molecular Formula
C24H27NO6
Molecular Weight
425.48
MDL Number
MFCD05663768
PubChem ID
10526402
Melting Point
110-117 ?C
Appearance
White crystalline powder
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-Nglu(OtBu)-OH
CAS Number
174799-89-4
Purity
≥ 99% (HPLC)
Molecular Formula
C24H27NO6
Molecular Weight
425.48
MDL Number
MFCD05663768
PubChem ID
10526402
Melting Point
110-117 ?C
Appearance
White crystalline 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

Fmoc-N-(tert-butyloxycarbonylethyl)glycine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without interfering with other functional groups. This is particularly beneficial in pharmaceutical research where precise peptide structures are crucial.
  • Drug Development: Its role in creating peptide-based drugs makes it valuable in the pharmaceutical industry. Researchers can design more effective therapeutic agents by utilizing this compound to enhance drug stability and efficacy.
  • Bioconjugation: The compound is used in bioconjugation processes, linking biomolecules to create targeted therapies. This application is significant in developing treatments for diseases like cancer, where targeted delivery of drugs is essential.
  • Research in Neuroscience: It is employed in the synthesis of neuropeptides, which are vital for understanding brain functions and developing treatments for neurological disorders. This application highlights its importance in advancing neuroscience research.
  • Custom Peptide Libraries: The chemical is instrumental in creating diverse peptide libraries for screening potential drug candidates. This allows researchers to explore a wide range of biological activities and discover new therapeutic options efficiently.

Citations