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Catalog Number:
29753
CAS Number:
141743-30-8
Fmoc- N -(2- terc -butoxietil)glicina
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-Nhser(tBu)-OH
Documents
$75.00 /100 mg
Tamaño
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Product Information

Fmoc-N-(2-tert-butoxyethyl)glycine is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino acids during solid-phase peptide synthesis. The tert-butoxyethyl side chain enhances its solubility and stability, making it particularly advantageous for researchers working on complex peptide sequences. Its unique structure allows for efficient coupling reactions, facilitating the synthesis of peptides with improved yields and purity.

In the pharmaceutical industry, Fmoc-N-(2-tert-butoxyethyl)glycine is instrumental in the development of peptide-based therapeutics, including those targeting various diseases. Its application extends to the creation of peptide libraries for drug discovery, where the ability to modify the side chain can lead to the identification of novel bioactive compounds. Researchers appreciate its compatibility with various coupling reagents and its ability to undergo deprotection under mild conditions, making it a preferred choice for those seeking reliable and efficient synthesis pathways.

Synonyms
Fmoc-Nhser(tBu)-OH
CAS Number
141743-30-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C23H27Nº 5
Molecular Weight
397.4
MDL Number
MFCD04112687
PubChem ID
2756166
Melting Point
101 - 108 °C (Literatura)
Appearance
Sólido blanco de bajo punto de fusión.
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-Nhser(tBu)-OH
CAS Number
141743-30-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C23H27Nº 5
Molecular Weight
397.4
MDL Number
MFCD04112687
PubChem ID
2756166
Melting Point
101 - 108 °C (Literatura)
Appearance
Sólido blanco de bajo punto de fusión.
Conditions
Conservar entre 0 y 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-(2-tert-butoxyethyl)glycine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides. Its protective Fmoc group allows for selective deprotection, facilitating the assembly of complex peptide chains.
  • Drug Development: In pharmaceutical research, it is used to create peptide-based drugs. Its stability and ease of modification make it an attractive option for developing new therapeutic agents.
  • Bioconjugation: The compound is employed in bioconjugation techniques, where it can be linked to other biomolecules, enhancing the delivery and efficacy of drugs or imaging agents.
  • Research in Neuroscience: It plays a role in studying neuropeptides, which are crucial for understanding brain functions and disorders. Researchers utilize it to create analogs that can modulate neuropeptide activity.
  • Material Science: Its properties are leveraged in the development of functional materials, such as hydrogels, which can be used in drug delivery systems or tissue engineering applications.

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