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Catalog Number:
15651
CAS Number:
511272-34-7
Fmoc-(R-3-amino-3-(2-hydroxyphenyl)propionic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-D-β-Phe(2-OH)-OH, Fmoc-D-β-o-Tyr-OH
Documents
$72.31 /100MG
Pack Size Availability Price
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Product Information

Fmoc-(R)-3-amino-3-(2-hydroxyphenyl)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 2-hydroxyphenyl group, enhances its reactivity and allows for the introduction of various functional groups, making it an ideal candidate for the development of bioactive peptides and pharmaceuticals.

Researchers and industry professionals can leverage Fmoc-(R)-3-amino-3-(2-hydroxyphenyl)propionic acid in the design of novel therapeutic agents, particularly in the fields of drug discovery and development. Its ability to facilitate the synthesis of complex peptide structures positions it as a valuable tool in the creation of targeted therapies and biologically active compounds. With its robust performance and compatibility with various coupling reagents, this compound stands out as a reliable choice for advancing peptide-based research and applications.

Synonyms
Fmoc-D-β-Phe(2-OH)-OH, Fmoc-D-β-o-Tyr-OH
CAS Number
511272-34-7
Purity
≥ 99% (HPLC)
Molecular Formula
C24H21NO5
Molecular Weight
403.43
MDL Number
MFCD03428015
PubChem ID
24902254
Melting Point
158-164 °C
Appearance
White powder
Optical Rotation
[a]D25 = +23 ± 2º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-D-β-Phe(2-OH)-OH, Fmoc-D-β-o-Tyr-OH
CAS Number
511272-34-7
Purity
≥ 99% (HPLC)
Molecular Formula
C24H21NO5
Molecular Weight
403.43
MDL Number
MFCD03428015
PubChem ID
24902254
Melting Point
158-164 °C
Appearance
White powder
Optical Rotation
[a]D25 = +23 ± 2º (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-(R)-3-amino-3-(2-hydroxyphenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in developing compounds that target specific receptors, enhancing therapeutic efficacy.
  • Bioconjugation: The compound can be used to create bioconjugates, linking biomolecules to drugs or imaging agents, which is essential in targeted therapy and diagnostics.
  • Research in Neuroscience: Its derivatives are explored for their potential neuroprotective effects, contributing to studies on neurodegenerative diseases and mental health treatments.
  • Material Science: The compound is also investigated for its role in developing smart materials, particularly those that respond to environmental stimuli, which can be applied in various industrial applications.

Citations