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Catalog Number:
15055
CAS Number:
917099-04-8
Fmoc-3-methoxy-D-phenlyalanine
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-D-Phe(3-OMe)-OH, Fmoc-3-methoxy-D-Phe-OH, (R-Fmoc-2-amino-3-(3-methoxyphenyl)propionic acid
Documents
$134.70 /100MG
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Product Information

Fmoc-3-methoxy-D-phenylalanine is a versatile amino acid derivative 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 groups during the synthesis of peptides. Its unique structure, characterized by the methoxy substitution on the phenyl ring, enhances its solubility and stability, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry.

In practical applications, Fmoc-3-methoxy-D-phenylalanine is employed in the synthesis of bioactive peptides and pharmaceuticals, contributing to advancements in targeted drug delivery systems and therapeutic agents. Its ability to facilitate the formation of complex peptide structures allows for the exploration of novel therapeutic pathways, particularly in the development of peptide-based drugs. Researchers appreciate its reliability and efficiency in peptide coupling reactions, making it a preferred choice for both academic and industrial applications.

Synonyms
Fmoc-D-Phe(3-OMe)-OH, Fmoc-3-methoxy-D-Phe-OH, (R-Fmoc-2-amino-3-(3-methoxyphenyl)propionic acid
CAS Number
917099-04-8
Purity
≥ 98% (HPLC)
Molecular Formula
C25H23NO5
Molecular Weight
417.46
MDL Number
MFCD04112685
PubChem ID
4712578
Appearance
White to off-white powder
Optical Rotation
[a]D25 = +30 ± 3º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-D-Phe(3-OMe)-OH, Fmoc-3-methoxy-D-Phe-OH, (R-Fmoc-2-amino-3-(3-methoxyphenyl)propionic acid
CAS Number
917099-04-8
Purity
≥ 98% (HPLC)
Molecular Formula
C25H23NO5
Molecular Weight
417.46
MDL Number
MFCD04112685
PubChem ID
4712578
Appearance
White to off-white powder
Optical Rotation
[a]D25 = +30 ± 3º (C=1 in DMF)
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-3-methoxy-D-phenylalanine 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, allowing researchers to create complex peptide chains efficiently.
  • Drug Development: Its unique structure makes it valuable in the design of pharmaceuticals, especially in developing drugs that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The Fmoc protecting group enables selective reactions, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in creating targeted drug delivery systems.
  • Research in Neuroscience: This compound can be used to study neurotransmitter interactions due to its structural similarity to amino acids, aiding in the development of neuroactive compounds.
  • Cosmetic Formulations: Its properties can be leveraged in the cosmetic industry for formulating products that require specific amino acid derivatives, enhancing skin absorption and effectiveness.

Citations