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Catalog Number:
41591
CAS Number:
215178-38-4
(S)-(+)-1-Fmoc-3-pyrrolidinol
Purity:
≥ 95%
Synonym(s):
(S)-1-(9-Fluorenylmethoxycarbonyl)-3-pyrrolidinol
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Product Information

(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.

Synonyms
(S)-1-(9-Fluorenylmethoxycarbonyl)-3-pyrrolidinol
CAS Number
215178-38-4
Purity
≥ 95%
Molecular Formula
C19H19NO3
Molecular Weight
309.36
MDL Number
MFCD01317842
PubChem ID
45356894
Melting Point
106 - 110 °C (dec.)
Appearance
White to off-white solid
Conditions
Store at RT
General Information
Synonyms
(S)-1-(9-Fluorenylmethoxycarbonyl)-3-pyrrolidinol
CAS Number
215178-38-4
Purity
≥ 95%
Molecular Formula
C19H19NO3
Molecular Weight
309.36
MDL Number
MFCD01317842
PubChem ID
45356894
Melting Point
106 - 110 °C (dec.)
Appearance
White to off-white solid
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(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.

Citations