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Catalog Number:
15627
CAS Number:
507472-28-8
Ácido Fmoc-( R -3-amino-3-(3-metilfenil)propiónico
Synonym(s):
Fmoc-D-β-Phe(3-Me)-OH, ( R -Fmoc-3-metil-β-fenilalanina
Documents
$206.60 /1G
Tamaño
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Product Information

Fmoc-(R)-3-amino-3-(3-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 groups during the synthesis of peptides. Its unique structure, characterized by the presence of a chiral center and a bulky aromatic side chain, enhances its utility in creating complex peptide sequences with improved stability and bioactivity. Researchers in pharmaceutical and biotechnological fields can leverage this compound for the development of novel therapeutics, particularly in the design of peptide-based drugs that target specific biological pathways.

The compound's ability to facilitate the synthesis of peptides with high purity and yield makes it an invaluable tool for chemists and biochemists. Its application extends to the production of peptide libraries for drug discovery, as well as in the development of targeted delivery systems. By incorporating Fmoc-(R)-3-amino-3-(3-methylphenyl)propionic acid into their workflows, professionals can enhance the efficiency of their research and development processes, ultimately leading to innovative solutions in medicine and biotechnology.

Synonyms
Fmoc-D-β-Phe(3-Me)-OH, ( R -Fmoc-3-metil-β-fenilalanina
CAS Number
507472-28-8
Molecular Formula
C25H23NO4
Molecular Weight
401.46
MDL Number
MFCD03428010
PubChem ID
22831637
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-D-β-Phe(3-Me)-OH, ( R -Fmoc-3-metil-β-fenilalanina
CAS Number
507472-28-8
Molecular Formula
C25H23NO4
Molecular Weight
401.46
MDL Number
MFCD03428010
PubChem ID
22831637
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-(3-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. Its Fmoc protecting group allows for selective deprotection during solid-phase peptide synthesis, making it easier for researchers to create complex peptide sequences.
  • Drug Development: It plays a significant role in the pharmaceutical industry, particularly in the design of peptide-based drugs. Its structural properties can enhance the bioactivity and stability of drug candidates.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps link biomolecules to therapeutic agents. This application is crucial in developing targeted drug delivery systems.
  • Research in Neuroscience: Researchers utilize this compound to study neuropeptides and their effects on the nervous system. Its unique structure allows for the exploration of new pathways in neurobiology.
  • Material Science: It is also applied in the development of functional materials, particularly in creating polymers with specific properties for use in various industrial applications.

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