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Catalog Number:
15652
CAS Number:
501015-31-2
Acide Fmoc-( S -3-amino-3-(2-hydroxyphényl)propionique)
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-β-Phe(2-OH)-OH, Fmoc-L-β- o -Tyr-OH
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$210.00 /1G
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Product Information

Fmoc-(S)-3-amino-3-(2-hydroxyphenyl)propionic acid is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This amino acid derivative 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 presence of a hydroxyl group on the aromatic ring, enhances its reactivity and solubility, making it an excellent choice for researchers focused on developing novel therapeutic peptides.

In addition to its role in peptide synthesis, Fmoc-(S)-3-amino-3-(2-hydroxyphenyl)propionic acid has potential applications in drug design and development, particularly in the creation of compounds targeting specific biological pathways. Its ability to facilitate the introduction of functional groups allows for the fine-tuning of molecular properties, which is crucial in optimizing drug efficacy and selectivity. Researchers in the pharmaceutical industry will find this compound invaluable for advancing their projects and achieving desired outcomes in peptide-based therapeutics.

Synonyms
Fmoc-L-β-Phe(2-OH)-OH, Fmoc-L-β- o -Tyr-OH
CAS Number
501015-31-2
Purity
≥ 98% (HPLC)
Molecular Formula
C 24 H 215
Molecular Weight
403.43
MDL Number
MFCD03427977
PubChem ID
24902254
Melting Point
155 - 159 °C
Appearance
White powder
Optical Rotation
[a]D25 = -22 ±2 °(C=1 in DMF)
Conditions
Conserver à 0-8°C
General Information
Synonyms
Fmoc-L-β-Phe(2-OH)-OH, Fmoc-L-β- o -Tyr-OH
CAS Number
501015-31-2
Purity
≥ 98% (HPLC)
Molecular Formula
C 24 H 215
Molecular Weight
403.43
MDL Number
MFCD03427977
PubChem ID
24902254
Melting Point
155 - 159 °C
Appearance
White powder
Optical Rotation
[a]D25 = -22 ±2 °(C=1 in DMF)
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-(S)-3-amino-3-(2-hydroxyphenyl)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, allowing researchers to create complex peptide structures efficiently.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing new drugs, especially those targeting specific receptors or pathways related to neurological disorders.
  • Bioconjugation: The chemical can be used in bioconjugation techniques, linking biomolecules to enhance drug delivery systems, which is crucial in targeted therapy.
  • Research in Neuroscience: It is applied in studies related to neurotransmitter activity, helping scientists understand the role of amino acids in brain function and potential treatments for mental health conditions.
  • Material Science: The compound can be incorporated into polymer matrices to create materials with specific properties, such as improved biocompatibility for medical devices.

Citations