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Catalog Number:
41591
CAS Number:
215178-38-4
( S )-(+)-1-Fmoc-3-pirrolidinol
Purity:
≥ 95%
Synonym(s):
( S )-1-(9-Fluorenilmetoxicarbonil)-3-pirrolidinol
Documents
$445.17 /5G
Tamaño
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Información del producto

(S)-(+)-1-Fmoc-3-pyrrolidinol is a versatile compound widely utilized in the field of organic synthesis and medicinal chemistry. This chiral building block is particularly valuable for its role in the development of peptide-based therapeutics and drug candidates. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group, allows for selective reactions, making it an essential tool for chemists engaged in the synthesis of complex molecules. Researchers appreciate its ability to enhance the solubility and stability of intermediates, facilitating smoother reaction processes and improving yields.

In addition to its applications in peptide synthesis, (S)-(+)-1-Fmoc-3-pyrrolidinol is also employed in the preparation of various bioactive compounds, including those targeting neurological disorders. Its chiral nature ensures that the resulting products possess the desired stereochemistry, which is crucial for biological activity. 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 in pharmaceuticals and related fields.

Número CAS
215178-38-4
Fórmula molecular
C 19 H 19 N º 3
Peso molecular
309.36
Número MDL
MFCD01317842
Punto de fusión
106 - 110 °C (descenso)
Condiciones
Tienda en RT
Información general
Número CAS
215178-38-4
Fórmula molecular
C 19 H 19 N º 3
Peso molecular
309.36
Número MDL
MFCD01317842
Punto de fusión
106 - 110 °C (descenso)
Condiciones
Tienda en RT
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

(S)-(+)-1-Fmoc-3-pyrrolidinol is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, enhancing the efficiency and selectivity of reactions, which is crucial for developing new pharmaceuticals.
  • Drug Development: Its application in medicinal chemistry allows researchers to create more effective drug candidates by modifying the structure of bioactive molecules, leading to improved therapeutic profiles.
  • Bioconjugation: The compound is used to facilitate the attachment of biomolecules, such as proteins or nucleic acids, to other molecules, which is essential in the development of targeted therapies and diagnostics.
  • Material Science: In polymer chemistry, it acts as a building block for creating advanced materials with specific properties, such as increased stability or enhanced biocompatibility.
  • Research in Neuroscience: Its derivatives are explored for potential applications in neuropharmacology, providing insights into the design of compounds that can affect neurological pathways.

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