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Catalog Number:
22698
CAS Number:
221352-86-9
Clorhidrato de 4- N -Fmoc-aminopiperidina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Clorhidrato de (Fmoc-4-amino)piperidina
Documents
$51.18 /250 mg
Tamaño
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Product Information

(Fmoc-4-amino)piperidine hydrochloride is a versatile compound widely utilized in the field of organic synthesis and medicinal chemistry. This compound serves as a crucial building block in the development of peptide-based therapeutics and drug discovery. Its unique Fmoc (fluorenylmethyloxycarbonyl) protective group allows for selective deprotection, making it an ideal choice for synthesizing complex peptides with high purity and yield. Researchers appreciate its stability and compatibility with various coupling reagents, facilitating streamlined synthesis processes.

In addition to its applications in peptide synthesis, (Fmoc-4-amino)piperidine hydrochloride is also employed in the development of novel pharmaceuticals targeting a range of diseases. Its ability to enhance the solubility and bioavailability of drug candidates makes it a valuable asset in formulation chemistry. With its proven track record in both academic and industrial settings, this compound stands out for its reliability and effectiveness in advancing research and development projects.

Synonyms
Clorhidrato de (Fmoc-4-amino)piperidina
CAS Number
221352-86-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C20H22N2O2 · HCl
Molecular Weight
358.87
MDL Number
MFCD01321024
PubChem ID
2756218
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Clorhidrato de (Fmoc-4-amino)piperidina
CAS Number
221352-86-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C20H22N2O2 · HCl
Molecular Weight
358.87
MDL Number
MFCD01321024
PubChem ID
2756218
Appearance
Sólido 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

(Fmoc-4-amino)piperidine hydrochloride is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids, which is essential for creating complex peptides.
  • Drug Development: Its structure aids in the design of novel pharmaceuticals, particularly in optimizing the pharmacological properties of drug candidates by enhancing their stability and bioavailability.
  • Bioconjugation: The compound is employed in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in developing targeted drug delivery systems.
  • Research in Neuroscience: It is used in the synthesis of compounds that interact with neurotransmitter systems, providing insights into neurological pathways and potential treatments for neurodegenerative diseases.
  • Material Science: The compound finds applications in the development of advanced materials, particularly in creating polymers with specific functionalities, enhancing their performance in various industrial applications.

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