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Catalog Number:
16684
CAS Number:
596096-27-4
Acide Fmoc-(2 S ,3 S )-3-amino-2-hydroxy-3-phénylpropionique
Purity:
≥ 99 % (HPLC)
Documents
$200.00 /100 mg
Taille
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Product Information

Fmoc-(2S,3S)-3-amino-2-hydroxy-3-phenylpropionic acid is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound, characterized by its fluorenylmethoxycarbonyl (Fmoc) protecting group, offers significant advantages in solid-phase peptide synthesis, allowing for efficient and selective coupling reactions. Its unique structure not only enhances stability during synthesis but also facilitates the incorporation of complex functionalities into peptides, making it an essential tool for researchers in medicinal chemistry and biochemistry.

The compound's properties make it particularly valuable in the design of bioactive peptides and pharmaceuticals. Its ability to form stable peptide bonds while maintaining the integrity of the amino acid side chains allows for the development of novel therapeutic agents. Additionally, Fmoc-(2S,3S)-3-amino-2-hydroxy-3-phenylpropionic acid can be employed in the synthesis of peptide-based drug candidates, offering potential applications in treating various diseases, including cancer and metabolic disorders. Researchers and industry professionals will find this compound indispensable for advancing their projects in peptide chemistry and drug formulation.

CAS Number
596096-27-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C 24 H 215
Molecular Weight
403.43
MDL Number
MFCD07363512
PubChem ID
53398433
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = 17 ± 2 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
CAS Number
596096-27-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C 24 H 215
Molecular Weight
403.43
MDL Number
MFCD07363512
PubChem ID
53398433
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = 17 ± 2 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 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-(2S,3S)-3-amino-2-hydroxy-3-phenylpropionic 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 addition of amino acids while preventing unwanted reactions.
  • Drug Development: It plays a crucial role in the design of peptide-based therapeutics, particularly in the development of drugs targeting specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation techniques, facilitating the attachment of peptides to other biomolecules, which is essential in creating targeted delivery systems in medicine.
  • Research in Neuroscience: Its structural properties make it valuable in studying neuropeptides, aiding researchers in understanding neurological functions and disorders.
  • Analytical Chemistry: The compound is employed in various analytical techniques, including chromatography, to separate and identify complex mixtures of peptides and proteins.

Citations