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Catalog Number:
15646
CAS Number:
501015-30-1
Fmoc-(S)-3-amino-3-(4-methoxyphenyl)propionic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-β-Phe(4-OMe)-OH, (S-Fmoc-4-methoxy-β-phenylalanine
Documents
$79.22 /250MG
Pack Size Availability Price
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Product Information

Fmoc-(S)-3-amino-3-(4-methoxyphenyl)propionic 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 amines during the synthesis of peptides. Its unique structure, characterized by the presence of a 4-methoxyphenyl group, enhances its stability and reactivity, making it an ideal choice for researchers focused on developing complex peptide sequences.

In practical applications, Fmoc-(S)-3-amino-3-(4-methoxyphenyl)propionic acid is particularly valuable in the pharmaceutical industry for the synthesis of bioactive peptides and therapeutic agents. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups allows for the efficient assembly of peptides with desired biological activities. This compound not only streamlines the synthesis process but also improves yields and purity, making it a preferred choice for both academic and industrial laboratories engaged in peptide research and development.

Synonyms
Fmoc-L-β-Phe(4-OMe)-OH, (S-Fmoc-4-methoxy-β-phenylalanine
CAS Number
501015-30-1
Purity
≥ 98% (HPLC)
Molecular Formula
C25H23NO5
Molecular Weight
417.46
MDL Number
MFCD03427976
PubChem ID
2759198
Appearance
White powder
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-L-β-Phe(4-OMe)-OH, (S-Fmoc-4-methoxy-β-phenylalanine
CAS Number
501015-30-1
Purity
≥ 98% (HPLC)
Molecular Formula
C25H23NO5
Molecular Weight
417.46
MDL Number
MFCD03427976
PubChem ID
2759198
Appearance
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-(4-methoxyphenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), where its Fmoc protecting group allows for selective deprotection and subsequent coupling reactions.
  • Drug Development: Its unique structure can be incorporated into drug candidates, enhancing bioactivity and specificity, particularly in the development of pharmaceuticals targeting neurological disorders.
  • Bioconjugation: The compound can be used in bioconjugation processes, facilitating the attachment of biomolecules to therapeutic agents, which is crucial in creating targeted drug delivery systems.
  • Research in Neuroscience: It is employed in studies related to neurotransmitter systems, where its analogs can help in understanding receptor interactions and signaling pathways.
  • Material Science: The compound is also explored in the development of functional materials, including hydrogels and coatings, due to its ability to modify surface properties and enhance material performance.

Citations