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Catalog Number:
07347
CAS Number:
221352-39-2
Boc-4-pipéridino-L-proline
Purity:
≥ 97 % (dosage)
Synonym(s):
Boc-(4-pipéridino)-L-Pro-OH, ( Acide S -Boc-4-pipéridino-pyrrolidine-2-carboxylique
Documents
$65.40 /1G
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Product Information

Boc-4-piperidino-L-proline is a versatile compound widely utilized in the fields of medicinal chemistry and pharmaceutical research. This amino acid derivative, characterized by its unique structure, serves as a valuable building block in the synthesis of peptide-based therapeutics. Its protective Boc (tert-butyloxycarbonyl) group enhances stability during chemical reactions, making it an ideal candidate for complex peptide synthesis. Researchers appreciate its role in developing novel drug candidates, particularly in the design of inhibitors and modulators for various biological targets.

In addition to its applications in drug development, Boc-4-piperidino-L-proline is also employed in the synthesis of ligands for receptor studies and in the formulation of advanced materials. Its favorable properties, such as solubility and reactivity, facilitate its use in diverse chemical reactions, allowing for the creation of tailored compounds that meet specific research needs. With its broad applicability and significant potential, Boc-4-piperidino-L-proline stands out as an essential tool for researchers aiming to innovate in the pharmaceutical landscape.

Synonyms
Boc-(4-pipéridino)-L-Pro-OH, ( Acide S -Boc-4-pipéridino-pyrrolidine-2-carboxylique
CAS Number
221352-39-2
Purity
≥ 97 % (dosage)
Molecular Formula
C15H26N2O4
Molecular Weight
298.38
MDL Number
MFCD01861211
PubChem ID
2755963
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-(4-pipéridino)-L-Pro-OH, ( Acide S -Boc-4-pipéridino-pyrrolidine-2-carboxylique
CAS Number
221352-39-2
Purity
≥ 97 % (dosage)
Molecular Formula
C15H26N2O4
Molecular Weight
298.38
MDL Number
MFCD01861211
PubChem ID
2755963
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-4-piperidino-L-proline is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in pharmaceutical research, enhancing the development of new therapeutic agents.
  • Drug Development: Its unique structure allows for the modification of drug candidates, improving their efficacy and bioavailability in the treatment of various diseases.
  • Biochemical Research: Used in the study of protein interactions and enzyme activity, it aids researchers in understanding complex biological systems.
  • Neuroscience Applications: The compound is explored for its potential in developing treatments for neurological disorders, providing insights into brain function and signaling pathways.
  • Custom Synthesis: Its versatility makes it a popular choice for custom synthesis projects in academic and industrial labs, addressing specific research needs efficiently.

Citations