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Catalog Number:
12634
CAS Number:
[" 494210-72-9"]
Fmoc-(1-Boc-piperidin-3-yl)-DL-glycine
Purity:
≥ 98% (HPLC)
Synonym(s):
N-Fmoc-DL-amino-(N-Boc-3-piperidinyl)aceticacid
Documents
$86.23 /25MG
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Product Information

Fmoc-(1-Boc-piperidin-3-yl)-DL-glycine is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique structure, incorporating a Boc (tert-butyloxycarbonyl) group on the piperidine ring, enhances its stability and solubility, making it an ideal choice for researchers working in medicinal chemistry and biochemistry.

This compound is particularly valuable in the synthesis of complex peptides and peptidomimetics, which are crucial for developing therapeutic agents. 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 molecules. Additionally, Fmoc-(1-Boc-piperidin-3-yl)-DL-glycine can be employed in the design of targeted drug delivery systems, providing a pathway for innovative treatments in various medical fields. Researchers and industry professionals will appreciate its reliability and effectiveness in advancing their projects.

Synonyms
N-Fmoc-DL-amino-(N-Boc-3-piperidinyl)aceticacid
CAS Number
[" 494210-72-9"]
Purity
≥ 98% (HPLC)
Molecular Formula
C27H32N2O6
Molecular Weight
480.6
MDL Number
MFCD02683126
PubChem ID
24729646
Appearance
White to off-white powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
N-Fmoc-DL-amino-(N-Boc-3-piperidinyl)aceticacid
CAS Number
[" 494210-72-9"]
Purity
≥ 98% (HPLC)
Molecular Formula
C27H32N2O6
Molecular Weight
480.6
MDL Number
MFCD02683126
PubChem ID
24729646
Appearance
White to off-white 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-(1-Boc-piperidin-3-yl)-DL-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 for drug development and biological studies.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in the development of compounds that target specific biological pathways.
  • Bioconjugation: The chemical is used in bioconjugation processes, linking biomolecules to enhance their stability and efficacy, which is crucial in creating targeted therapies.
  • Research in Neuroscience: Due to its piperidine moiety, it is valuable in neuroscience research for developing compounds that can interact with neurotransmitter systems.
  • Custom Synthesis: It is often employed in custom synthesis projects where specific modifications are needed to optimize the properties of compounds for various applications.

Citations