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Catalog Number:
07360
CAS Number:
811841-89-1
1-Fmoc-4-aminopiperidine hydrochloride
Documents
$79.22 /250MG
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Product Information

1-Fmoc-4-aminopiperidine hydrochloride is a versatile compound widely utilized in the field of peptide synthesis and medicinal chemistry. This protected amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) group, which serves as a temporary protective group during the synthesis of peptides. Its unique structure allows for selective deprotection, making it an essential building block for researchers aiming to create complex peptide sequences. The compound's hydrochloride form enhances its solubility, facilitating its use in various organic reactions and applications.

In addition to its role in peptide synthesis, 1-Fmoc-4-aminopiperidine hydrochloride is also valuable in drug discovery and development, particularly in the design of novel therapeutic agents. Its ability to form stable interactions with biological targets makes it a promising candidate for further exploration in pharmaceutical applications. Researchers appreciate its reliability and efficiency, which can significantly streamline the synthesis process compared to other similar compounds. With its robust profile, this compound is an indispensable tool for professionals in the pharmaceutical and biotechnology sectors.

CAS Number
811841-89-1
Molecular Formula
C20H25N2O2Cl3
Molecular Weight
431.78
MDL Number
MFCD03001675
PubChem ID
2756229
Melting Point
172-184 ?C
Appearance
White powder
Conditions
Store at 0-8°C
General Information
CAS Number
811841-89-1
Molecular Formula
C20H25N2O2Cl3
Molecular Weight
431.78
MDL Number
MFCD03001675
PubChem ID
2756229
Melting Point
172-184 ?C
Appearance
White powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1-Fmoc-4-aminopiperidine hydrochloride is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as an important building block in the synthesis of peptides. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection, facilitating the stepwise assembly of peptide chains.
  • Drug Development: In pharmaceutical research, it plays a crucial role in developing new drug candidates, particularly in the design of compounds targeting specific biological pathways, enhancing efficacy and selectivity.
  • Bioconjugation: The compound is used in bioconjugation processes, where it can be linked to biomolecules, aiding in the creation of targeted drug delivery systems that improve therapeutic outcomes.
  • Research in Neuroscience: Its structure is relevant in studies related to neurotransmitter systems, providing insights into the development of treatments for neurological disorders.
  • Custom Synthesis: Researchers appreciate its versatility for custom synthesis projects, allowing for the creation of novel compounds tailored to specific research needs, which can lead to breakthroughs in various fields.

Citations