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Catalog Number:
15066
CAS Number:
141743-16-0
Fmoc-N-(tert-butyloxycarbonylmethyl)glycine
Purity:
≥ 98% (HPLC)
Documents
$86.23 /250MG
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Product Information

Fmoc-N-(tert-butyloxycarbonylmethyl)glycine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its tert-butyloxycarbonyl (Boc) moiety enhances stability and solubility, making it an ideal choice for researchers focused on complex peptide structures. The unique combination of these protective groups allows for efficient coupling reactions, facilitating the synthesis of various bioactive peptides and pharmaceuticals.

In practical applications, Fmoc-N-(tert-butyloxycarbonylmethyl)glycine is particularly valuable in the fields of medicinal chemistry and biochemistry, where it serves as a building block for the development of peptide-based therapeutics. Its robust nature and compatibility with automated synthesizers streamline the peptide synthesis process, enabling researchers to produce high-purity peptides with greater efficiency. This compound stands out among similar derivatives due to its enhanced stability and ease of use, making it a preferred choice for professionals in the pharmaceutical and research industries.

CAS Number
141743-16-0
Purity
≥ 98% (HPLC)
Molecular Formula
C23H25NO6
Molecular Weight
411.45
MDL Number
MFCD05663767
PubChem ID
10573674
Melting Point
115-120 ?C
Appearance
White crystalline powder
Conditions
Store at 0-8 °C
General Information
CAS Number
141743-16-0
Purity
≥ 98% (HPLC)
Molecular Formula
C23H25NO6
Molecular Weight
411.45
MDL Number
MFCD05663767
PubChem ID
10573674
Melting Point
115-120 ?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-butyloxycarbonylmethyl)glycine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as an important building block in the synthesis of peptides, allowing researchers to create complex molecules for drug development and therapeutic applications.
  • Drug Discovery: Its unique structure aids in the design of novel pharmaceuticals, particularly in the field of cancer research, where targeted therapies are essential.
  • Bioconjugation: The compound is used in bioconjugation processes, facilitating the attachment of biomolecules to drugs, enhancing their efficacy and specificity.
  • Analytical Chemistry: It plays a role in analytical methods, such as chromatography, helping to separate and identify compounds in complex mixtures.
  • Research in Neuroscience: Its derivatives are explored in neuroscience research to understand peptide interactions in the brain, potentially leading to new treatments for neurological disorders.

Citations