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Catalog Number:
22665
CAS Number:
154938-68-8
Ácido 3-(1-Fmoc-piperidin-4-il)propiónico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ácido N -Fmoc-4-piperidinapropiónico
Documents
$134.70 /100 mg
Tamaño
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Product Information

3-(1-Fmoc-piperidin-4-yl)propionic acid is a versatile compound widely utilized in the field of peptide synthesis and drug development. This amino acid derivative features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which is crucial for the selective protection of amines during the synthesis of peptides. Its unique structure allows for efficient coupling reactions, making it an essential building block for creating complex peptide sequences. Researchers and industry professionals appreciate its stability and compatibility with various coupling reagents, which enhances the overall yield and purity of synthesized peptides.

In addition to its role in peptide synthesis, 3-(1-Fmoc-piperidin-4-yl)propionic acid has potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting neurological disorders. Its piperidine moiety contributes to its bioactivity, making it a valuable candidate for further exploration in drug design. The compound's ability to facilitate the synthesis of bioactive peptides positions it as a key player in advancing therapeutic research and development, providing researchers with a reliable tool for innovative solutions in drug discovery.

Synonyms
Ácido N -Fmoc-4-piperidinapropiónico
CAS Number
154938-68-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C23H25NO4
Molecular Weight
379.46
MDL Number
MFCD02179125
PubChem ID
2756122
Melting Point
113-119 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido N -Fmoc-4-piperidinapropiónico
CAS Number
154938-68-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C23H25NO4
Molecular Weight
379.46
MDL Number
MFCD02179125
PubChem ID
2756122
Melting Point
113-119 ?C
Appearance
Polvo blanco
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

3-(1-Fmoc-piperidin-4-yl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex peptide structures with high purity.
  • Drug Development: It is used in the pharmaceutical industry for developing new drug candidates, especially those targeting neurological disorders, due to its ability to modify peptide properties effectively.
  • Bioconjugation: The chemical is employed in bioconjugation processes, where it helps to attach biomolecules to surfaces or other molecules, enhancing the functionality of therapeutic agents.
  • Research in Neuroscience: This compound is significant in neuroscience research, facilitating the study of receptor interactions and signaling pathways, which is crucial for understanding brain function and developing treatments.
  • Custom Synthesis: It is also valuable for custom synthesis projects in laboratories, providing researchers with a versatile tool for creating tailored compounds for specific experimental needs.

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