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Catalog Number:
33661
Fmoc-(2R,3R-3-amino-2-hydroxy-3-p-tolyl-propionic acid
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$100.05 /25MG
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Product Information

Fmoc-(2R,3R)-3-amino-2-hydroxy-3-p-tolyl-propionic acid is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which facilitates the selective protection of the amino group during the synthesis of peptides. Its chiral centers enhance its relevance in the creation of biologically active compounds, making it a valuable tool for researchers in medicinal chemistry and pharmaceutical applications.

The compound's ability to form stable peptide bonds and its compatibility with various coupling reagents make it an excellent choice for solid-phase peptide synthesis. Additionally, its structural properties allow for the incorporation of hydrophobic side chains, which can improve the solubility and bioavailability of peptides. Researchers and industry professionals can leverage Fmoc-(2R,3R)-3-amino-2-hydroxy-3-p-tolyl-propionic acid to develop novel therapeutics and optimize existing peptide-based drugs, thus enhancing their efficacy and therapeutic potential.

Molecular Formula
C25H23NO5
Molecular Weight
417.45
MDL Number
MFCD07363630
Conditions
Store at 2 - 8 °C
General Information
Molecular Formula
C25H23NO5
Molecular Weight
417.45
MDL Number
MFCD07363630
Conditions
Store at 2 - 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-3-p-tolyl-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), allowing for the creation of complex peptide structures with high purity.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing new drugs, especially those targeting specific biological pathways, enhancing efficacy and reducing side effects.
  • Bioconjugation: The compound can be used in bioconjugation techniques to attach biomolecules to surfaces or other compounds, facilitating the development of targeted drug delivery systems and diagnostic tools.
  • Research in Neuroscience: It plays a role in the study of neurotransmitter systems, aiding researchers in understanding the mechanisms of action for various neurological disorders.
  • Protein Engineering: This chemical is instrumental in protein engineering applications, allowing scientists to modify proteins for improved stability and functionality in various biotechnological applications.

Citations