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Catalog Number:
16846
CAS Number:
1117321-94-6
Fmoc-(2R,3R)-3-amino-2-hydroxy-4-phenylbutyric acid
Purity:
≥ 98% (HPLC)
Documents
$141.41 /25MG
Pack Size Availability Price
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Product Information

Fmoc-(2R,3R)-3-amino-2-hydroxy-4-phenylbutyric acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a fluorenylmethyloxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure, characterized by a chiral center, enhances its applicability in the creation of biologically active compounds, making it a valuable asset in pharmaceutical research and development.

Researchers appreciate its ability to facilitate the formation of complex peptide structures while maintaining high levels of purity and yield. This compound is particularly useful in the synthesis of peptides that require specific stereochemistry, which is crucial for their biological activity. Additionally, its stability under various reaction conditions allows for greater flexibility in experimental design. Fmoc-(2R,3R)-3-amino-2-hydroxy-4-phenylbutyric acid stands out in the field of medicinal chemistry, offering a reliable option for those looking to innovate in drug design and peptide-based therapies.

CAS Number
1117321-94-6
Purity
≥ 98% (HPLC)
Molecular Formula
C25H23NO5
Molecular Weight
417.45
MDL Number
MFCD02682592
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
CAS Number
1117321-94-6
Purity
≥ 98% (HPLC)
Molecular Formula
C25H23NO5
Molecular Weight
417.45
MDL Number
MFCD02682592
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-(2R,3R)-3-amino-2-hydroxy-4-phenylbutyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective formation of peptide bonds while preventing unwanted reactions.
  • Drug Development: Its unique structure makes it valuable in the design of novel pharmaceuticals, particularly in developing compounds with enhanced bioactivity and specificity.
  • Biotechnology: It is used in the modification of proteins and peptides, facilitating the study of protein interactions and functions in various biological systems.
  • Material Science: This chemical can be incorporated into polymer matrices to create materials with specific properties, such as improved mechanical strength or biocompatibility.
  • Research in Neuroscience: Its derivatives are explored for potential applications in neuroprotective agents, contributing to studies aimed at treating neurodegenerative diseases.

Citations