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Catalog Number:
15302
CAS Number:
269398-91-6
Fmoc-(R-3-amino-4-(2-naphthyl)butyric acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-D-β-HomoAla(2-naphthyl)-OH, Fmoc-(2-naphthyl)-D-β-homoalanine
Documents
$154.93 /250MG
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Product Information

Fmoc-(R)-3-amino-4-(2-naphthyl)butyric 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 naphthyl group, enhances the compound's hydrophobic properties, making it particularly useful in the design of bioactive peptides and pharmaceuticals. Researchers appreciate its stability and compatibility with various coupling reagents, which facilitates efficient synthesis processes.

In addition to its role in peptide synthesis, Fmoc-(R)-3-amino-4-(2-naphthyl)butyric acid has shown potential in the development of novel therapeutic agents targeting specific biological pathways. Its application extends to the fields of medicinal chemistry and biochemistry, where it serves as a critical intermediate in the creation of compounds with enhanced biological activity. The ability to modify the naphthyl group further allows for the fine-tuning of pharmacokinetic properties, making it an attractive option for researchers aiming to optimize drug efficacy and safety.

Synonyms
Fmoc-D-β-HomoAla(2-naphthyl)-OH, Fmoc-(2-naphthyl)-D-β-homoalanine
CAS Number
269398-91-6
Purity
≥ 98% (HPLC)
Molecular Formula
C29H25NO4
Molecular Weight
451.52
MDL Number
MFCD01860938
PubChem ID
17972039
Appearance
Off-white powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-D-β-HomoAla(2-naphthyl)-OH, Fmoc-(2-naphthyl)-D-β-homoalanine
CAS Number
269398-91-6
Purity
≥ 98% (HPLC)
Molecular Formula
C29H25NO4
Molecular Weight
451.52
MDL Number
MFCD01860938
PubChem ID
17972039
Appearance
Off-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)-3-amino-4-(2-naphthyl)butyric 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 modification of amino acids without affecting other functional groups.
  • Drug Development: Its unique structure is beneficial in the design of novel pharmaceuticals, particularly in developing compounds that target specific biological pathways.
  • Bioconjugation: The chemical is used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in diagnostics and therapeutic applications.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems, aiding researchers in understanding the effects of amino acids on brain function and behavior.
  • Material Science: The compound is explored in the development of new materials, particularly those that require specific interactions at the molecular level, enhancing the performance of polymers and composites.

Citations