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Catalog Number:
15636
CAS Number:
501015-28-7
Fmoc-(S-3-amino-3-(2-methoxyphenyl)propionic acid
Purity:
≥ 95% (NMR)
Synonym(s):
Fmoc-L-β-Phe(2-OMe)-OH, (S-Fmoc-2-methoxy-β-phenylalanine
Documents
$72.31 /250MG
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Product Information

Fmoc-(S)-3-amino-3-(2-methoxyphenyl)propionic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique structure, characterized by the presence of a methoxyphenyl group, enhances its solubility and stability, making it an ideal choice for researchers looking to develop complex peptide sequences with improved yields and purity.

In the pharmaceutical industry, this compound is particularly valuable for the development of bioactive peptides and drug candidates. Its application extends to the synthesis of peptide-based therapeutics, where it aids in the creation of compounds with specific biological activities. Researchers appreciate its ability to facilitate the introduction of functional groups, allowing for the fine-tuning of peptide properties. With its favorable characteristics, Fmoc-(S)-3-amino-3-(2-methoxyphenyl)propionic acid stands out as a crucial reagent for advancing peptide chemistry and drug discovery.

Synonyms
Fmoc-L-β-Phe(2-OMe)-OH, (S-Fmoc-2-methoxy-β-phenylalanine
CAS Number
501015-28-7
Purity
≥ 95% (NMR)
Molecular Formula
C25H23NO5
Molecular Weight
417.46
MDL Number
MFCD03427974
PubChem ID
22831634
Appearance
White to off-white powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-β-Phe(2-OMe)-OH, (S-Fmoc-2-methoxy-β-phenylalanine
CAS Number
501015-28-7
Purity
≥ 95% (NMR)
Molecular Formula
C25H23NO5
Molecular Weight
417.46
MDL Number
MFCD03427974
PubChem ID
22831634
Appearance
White to off-white powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(S)-3-amino-3-(2-methoxyphenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting the overall structure. This is crucial in developing pharmaceuticals and biologically active compounds.
  • Drug Development: Its unique structure aids in designing new drug candidates, particularly in the field of neuropharmacology, where modifications can enhance the efficacy and selectivity of therapeutic agents.
  • Bioconjugation: The compound is used in bioconjugation processes, linking biomolecules to improve drug delivery systems, which can lead to targeted therapies with reduced side effects.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems, helping researchers understand the mechanisms of action for various neuroactive substances, which is vital for developing treatments for neurological disorders.
  • Material Science: The compound's properties can be leveraged in creating novel materials, such as polymers or hydrogels, that have applications in drug delivery and tissue engineering.

Citations