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Catalog Number:
15060
CAS Number:
269078-79-7
Fmoc-(R,S-3-amino-3-(biphenyl)propionic acid
Purity:
≥ 97% (HPLC)
Synonym(s):
Fmoc-DL-3-(4-diphenyl)-3-amino-propionic acid
Documents
$113.87 /250MG
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Product Information

Fmoc-(R,S)-3-amino-3-(biphenyl)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 biphenyl structure enhances the compound's hydrophobic interactions, making it particularly useful in the design of bioactive peptides and pharmaceuticals. Researchers appreciate its ability to facilitate the formation of stable peptide bonds, which is crucial in the development of therapeutic agents targeting various diseases.

In addition to its role in peptide synthesis, Fmoc-(R,S)-3-amino-3-(biphenyl)propionic acid has potential applications in materials science, particularly in the development of functional polymers and nanomaterials. Its structural properties allow for the creation of innovative materials with tailored functionalities. This compound stands out among similar products due to its enhanced stability and compatibility with various coupling reagents, making it a preferred choice for professionals in both academic and industrial settings.

Synonyms
Fmoc-DL-3-(4-diphenyl)-3-amino-propionic acid
CAS Number
269078-79-7
Purity
≥ 97% (HPLC)
Molecular Formula
C30H25NO4
Molecular Weight
463.17
MDL Number
MFCD02179646
PubChem ID
2756162
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-DL-3-(4-diphenyl)-3-amino-propionic acid
CAS Number
269078-79-7
Purity
≥ 97% (HPLC)
Molecular Formula
C30H25NO4
Molecular Weight
463.17
MDL Number
MFCD02179646
PubChem ID
2756162
Appearance
White powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(R,S)-3-amino-3-(biphenyl)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: It is used in the development of pharmaceutical compounds, especially in designing peptides that can act as drug candidates, enhancing bioactivity and specificity.
  • Bioconjugation: The chemical is valuable in bioconjugation techniques, where it helps attach biomolecules to surfaces or other molecules, improving the efficacy of diagnostics and therapeutics.
  • Research in Neuroscience: Its unique structure makes it useful in studying neuroactive peptides, contributing to research on neurological disorders and potential treatments.
  • Material Science: The compound is also explored in the development of advanced materials, such as hydrogels, due to its ability to influence polymer properties and interactions.

Citations