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Catalog Number:
22759
CAS Number:
1310680-23-9
Acide S -Fmoc-5,5-diméthyl-pyrrolidine-2-carboxylique
Purity:
≥ 98 % (HPLC)
Synonym(s):
( S -Fmoc-5,5-diméthyl-Pro-OH
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$154.93 /25 mg
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Product Information

(S)-Fmoc-5,5-dimethyl-pyrrolidine-2-carboxylic acid is a versatile building block widely utilized in peptide synthesis and drug development. 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, characterized by the presence of two methyl groups on the pyrrolidine ring, enhances its stability and solubility, making it an ideal choice for researchers looking to streamline their synthesis processes.

In the pharmaceutical industry, (S)-Fmoc-5,5-dimethyl-pyrrolidine-2-carboxylic acid is particularly valuable for the synthesis of bioactive peptides and complex molecules, facilitating the development of new therapeutics. Its ability to provide high yields and purity in peptide synthesis positions it as a preferred reagent among chemists. Additionally, its compatibility with various coupling reagents and solvents further enhances its utility in diverse chemical environments. Researchers can leverage this compound to accelerate their projects while ensuring the integrity and efficacy of their synthesized products.

Synonyms
( S -Fmoc-5,5-diméthyl-Pro-OH
CAS Number
1310680-23-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 22 H 234
Molecular Weight
365.43
MDL Number
MFCD09952631
PubChem ID
75084929
Appearance
Poudre blanche
Optical Rotation
[a] D 20
Conditions
Conserver à 0-8 °C
General Information
Synonyms
( S -Fmoc-5,5-diméthyl-Pro-OH
CAS Number
1310680-23-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 22 H 234
Molecular Weight
365.43
MDL Number
MFCD09952631
PubChem ID
75084929
Appearance
Poudre blanche
Optical Rotation
[a] D 20
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

(S)-Fmoc-5,5-dimethyl-pyrrolidine-2-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions while preventing unwanted side reactions. Its stability and ease of removal make it a preferred choice in organic chemistry.
  • Drug Development: In pharmaceutical research, it is used to create complex molecules that can lead to new drug candidates. Its unique structure can enhance the bioavailability and efficacy of therapeutic agents.
  • Bioconjugation: The compound is valuable in bioconjugation processes, where it helps in attaching biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Material Science: It finds applications in the development of advanced materials, particularly in creating polymers with specific properties that can be used in coatings or biomedical devices.
  • Research in Neuroscience: The compound is explored for its potential in studying neurological pathways, providing insights into brain chemistry and aiding in the development of treatments for neurological disorders.

Citations