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Catalog Number:
15074
CAS Number:
193693-66-2
Fmoc-(3 S -β-Pro-OH
Purity:
≥ 95 % (RMN)
Synonym(s):
Acide Fmoc-(3 S -1-pyrrolidine-3-carboxylique
Documents
$100.05 /100 mg
Taille
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Product Information

Fmoc-(3S)-b-Pro-OH is a versatile building block widely utilized in peptide synthesis, particularly in the development of pharmaceutical compounds and bioconjugates. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino acids during solid-phase peptide synthesis. Its unique structure enhances stability and solubility, making it an ideal choice for researchers focused on synthesizing complex peptides with high purity and yield.

In addition to its role in peptide synthesis, Fmoc-(3S)-b-Pro-OH has shown potential in various applications, including drug development and the creation of novel biomaterials. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups makes it a preferred choice among chemists and biochemists. Researchers can leverage this compound to streamline their workflows, reduce reaction times, and improve overall efficiency in peptide assembly, ultimately leading to advancements in therapeutic development and biomolecular research.

Synonyms
Acide Fmoc-(3 S -1-pyrrolidine-3-carboxylique
CAS Number
193693-66-2
Purity
≥ 95 % (RMN)
Molecular Formula
C 20 H 194
Molecular Weight
337.37
MDL Number
MFCD04112695
PubChem ID
5223225
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Acide Fmoc-(3 S -1-pyrrolidine-3-carboxylique
CAS Number
193693-66-2
Purity
≥ 95 % (RMN)
Molecular Formula
C 20 H 194
Molecular Weight
337.37
MDL Number
MFCD04112695
PubChem ID
5223225
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

Fmoc-(3S)-b-Pro-OH 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 without interfering with other functional groups.
  • Drug Development: Its application in the synthesis of peptide-based drugs enhances the stability and bioavailability of therapeutic agents, making it valuable in pharmaceutical research.
  • Biotechnology: Used in the production of peptide vaccines, it helps in the design of immunogenic peptides that can stimulate an immune response, crucial for vaccine development.
  • Research in Neuroscience: This compound is employed in creating neuropeptides, which are important for studying neural signaling and potential treatments for neurological disorders.
  • Custom Synthesis Services: Many chemical suppliers offer tailored synthesis of this compound, catering to specific research needs, which can save time and resources for researchers.

Citations