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Catalog Number:
15691
CAS Number:
501015-38-9
Acide Fmoc-( S -3-amino-3-(3,5-diméthoxyphényl)propionique)
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-β-Phe(3,5-diméthoxy)-OH, ( S -Fmoc-3,5-diméthoxy-β-phénylalanine
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Product Information

Fmoc-(S)-3-amino-3-(3,5-dimethoxyphenyl)propionic acid is a valuable building block in peptide synthesis, particularly in the field of medicinal chemistry and drug development. This compound, known for its high purity and stability, serves as a crucial intermediate for the preparation of various bioactive peptides. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group, allows for selective deprotection under mild conditions, making it an ideal choice for researchers looking to streamline their synthesis processes.

The compound's specific application in the synthesis of peptide-based therapeutics highlights its importance in the pharmaceutical industry. Researchers utilize Fmoc-(S)-3-amino-3-(3,5-dimethoxyphenyl)propionic acid to create peptides that target specific biological pathways, potentially leading to innovative treatments for various diseases. Its compatibility with solid-phase peptide synthesis (SPPS) further enhances its utility, allowing for efficient and reproducible peptide assembly. With its favorable properties and practical applications, this compound is a must-have for any laboratory focused on peptide chemistry.

Synonyms
Fmoc-L-β-Phe(3,5-diméthoxy)-OH, ( S -Fmoc-3,5-diméthoxy-β-phénylalanine
CAS Number
501015-38-9
Purity
≥ 98% (HPLC)
Molecular Formula
C 26 H 256
Molecular Weight
447.49
MDL Number
MFCD03427984
PubChem ID
22309351
Appearance
White powder
Conditions
Conserver à 0-8°C
General Information
Synonyms
Fmoc-L-β-Phe(3,5-diméthoxy)-OH, ( S -Fmoc-3,5-diméthoxy-β-phénylalanine
CAS Number
501015-38-9
Purity
≥ 98% (HPLC)
Molecular Formula
C 26 H 256
Molecular Weight
447.49
MDL Number
MFCD03427984
PubChem ID
22309351
Appearance
White powder
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-(S)-3-amino-3-(3,5-dimethoxyphenyl)propionic acid 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 while preventing unwanted reactions.
  • Drug Development: It plays a crucial role in the design of peptide-based drugs, particularly in enhancing the stability and bioavailability of therapeutic peptides.
  • Bioconjugation: The compound is used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Research in Neuroscience: Its derivatives are explored in studies related to neuroactive peptides, contributing to the understanding of neurological disorders and potential treatments.
  • Material Science: The compound is applied in the development of novel materials for drug delivery systems, improving the efficiency of therapeutic agents in clinical applications.

Citations