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Catalog Number:
15621
CAS Number:
507472-27-7
Ácido Fmoc-( R -3-amino-3-(2-metilfenil)propiónico
Synonym(s):
Fmoc-D-β-Phe(2-Me)-OH, ( R -Fmoc-2-metil-β-fenilalanina
Documents
$206.60 /1G
Tamaño
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Product Information

Fmoc-(R)-3-amino-3-(2-methylphenyl)propionic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino acids during solid-phase peptide synthesis. Its unique structure, characterized by the presence of a 2-methylphenyl group, enhances its stability and reactivity, making it an ideal choice for researchers focused on developing complex peptides with specific functionalities.

In the pharmaceutical industry, this compound plays a crucial role in the synthesis of bioactive peptides, which are vital for therapeutic applications. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups allows for the creation of tailored peptides that can target specific biological pathways. Researchers have successfully employed Fmoc-(R)-3-amino-3-(2-methylphenyl)propionic acid in the development of novel drug candidates, showcasing its potential in advancing medicinal chemistry and biochemistry.

Synonyms
Fmoc-D-β-Phe(2-Me)-OH, ( R -Fmoc-2-metil-β-fenilalanina
CAS Number
507472-27-7
Molecular Formula
C25H23NO4
Molecular Weight
401.46
MDL Number
MFCD03428009
PubChem ID
22831633
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-D-β-Phe(2-Me)-OH, ( R -Fmoc-2-metil-β-fenilalanina
CAS Number
507472-27-7
Molecular Formula
C25H23NO4
Molecular Weight
401.46
MDL Number
MFCD03428009
PubChem ID
22831633
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(R)-3-amino-3-(2-methylphenyl)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 sequences with high purity.
  • Drug Development: Its unique structure makes it valuable in the pharmaceutical industry for designing novel drug candidates, especially in targeting specific biological pathways.
  • Bioconjugation: The chemical is used in bioconjugation processes, facilitating the attachment of biomolecules to therapeutic agents, enhancing their efficacy and specificity.
  • Research in Neuroscience: Due to its structural properties, it is applied in studies related to neuropeptides, aiding in the understanding of neural signaling and potential treatments for neurological disorders.
  • Material Science: This compound is also explored in the development of advanced materials, such as hydrogels, which can be utilized in drug delivery systems and tissue engineering applications.

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