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Catalog Number:
33655
Acide Fmoc-(2 R ,3 R -3-amino-2-hydroxy-3- m -tolyl-propionique
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$100.05 /25 mg
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Product Information

Fmoc-(2R,3R)-3-amino-2-hydroxy-3-m-tolyl-propionic acid is a valuable building block in peptide synthesis, particularly in the development of peptide-based therapeutics and research applications. This compound features a protected amino acid structure that allows for selective coupling reactions, making it an essential tool for chemists working in the fields of medicinal chemistry and biochemistry. Its unique Fmoc (9-fluorenylmethoxycarbonyl) protection group facilitates easy removal under mild conditions, ensuring that the integrity of the peptide chain is maintained during synthesis.

This compound is particularly useful in the synthesis of complex peptides and proteins, where precise control over amino acid sequences is crucial. Researchers have utilized Fmoc-(2R,3R)-3-amino-2-hydroxy-3-m-tolyl-propionic acid to create bioactive peptides with enhanced stability and activity, which can be applied in drug development, vaccine formulation, and various biochemical assays. Its ability to enhance solubility and bioavailability makes it a preferred choice for developing therapeutic agents. With its robust performance and versatility, this compound stands out as a key ingredient for advancing peptide synthesis and related applications.

Molecular Formula
C 25 H 235
Molecular Weight
417.45
MDL Number
MFCD07363624
Conditions
Conserver entre 2 et 8 °C
General Information
Molecular Formula
C 25 H 235
Molecular Weight
417.45
MDL Number
MFCD07363624
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-(2R,3R)-3-amino-2-hydroxy-3-m-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, allowing for the creation of complex peptide sequences with high purity.
  • Drug Development: It is used in the development of pharmaceutical compounds, especially in creating targeted therapies where specific amino acid configurations are crucial for efficacy.
  • Bioconjugation: The chemical is applied in bioconjugation processes, enabling the attachment of biomolecules to drugs or imaging agents, enhancing their therapeutic or diagnostic capabilities.
  • Research in Neuroscience: It plays a role in studies related to neurotransmitter systems, helping researchers understand the structure-activity relationships of neuroactive compounds.
  • Material Science: The compound is also explored in the development of novel materials, particularly in creating functional polymers that can respond to environmental stimuli.

Citations