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Catalog Number:
12636
CAS Number:
204058-24-2
Fmoc-1(1-Boc-pipéridin-4-yl)-DL-glycine
Purity:
≥ 95 % (HPLC)
Synonym(s):
Acide N -Fmoc-DL-amino-( N -Boc-4-pipéridinyl)acétique
Documents
$172.96 /100 mg
Taille
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Product Information

Fmoc-1(1-Boc-piperidin-4-yl)-DL-glycine is a versatile amino acid derivative 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 groups during the synthesis of peptides. Its unique structure, incorporating a Boc (tert-butyloxycarbonyl) group, enhances stability and solubility, making it an ideal choice for researchers focused on complex peptide sequences.

In practical applications, Fmoc-1(1-Boc-piperidin-4-yl)-DL-glycine is particularly valuable in the pharmaceutical industry for the development of peptide-based therapeutics. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups allows for the efficient assembly of biologically active peptides. Additionally, this compound is instrumental in the synthesis of cyclic peptides and other advanced materials, providing researchers with a reliable tool for exploring novel therapeutic avenues.

Synonyms
Acide N -Fmoc-DL-amino-( N -Boc-4-pipéridinyl)acétique
CAS Number
204058-24-2
Purity
≥ 95 % (HPLC)
Molecular Formula
C27H32N2O6
Molecular Weight
480.6
MDL Number
MFCD01860500
PubChem ID
24729637
Appearance
Solide blanc
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Acide N -Fmoc-DL-amino-( N -Boc-4-pipéridinyl)acétique
CAS Number
204058-24-2
Purity
≥ 95 % (HPLC)
Molecular Formula
C27H32N2O6
Molecular Weight
480.6
MDL Number
MFCD01860500
PubChem ID
24729637
Appearance
Solide blanc
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-1(1-Boc-piperidin-4-yl)-DL-glycine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as an important building block in the synthesis of peptides, allowing for the introduction of specific amino acid sequences in drug development and research.
  • Drug Development: Its unique structure aids in the formulation of novel pharmaceuticals, particularly in creating compounds with improved bioavailability and efficacy.
  • Bioconjugation: It is used in bioconjugation techniques, linking biomolecules like proteins and antibodies to enhance therapeutic properties and targeting capabilities in cancer treatments.
  • Research in Neuroscience: The piperidine moiety is beneficial in studying neuroactive compounds, providing insights into neurotransmitter systems and potential treatments for neurological disorders.
  • Custom Synthesis: Researchers in academia and industry leverage its properties for custom synthesis projects, enabling the development of tailored compounds for specific applications.

Citations