💛 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
15068
CAS Number:
683217-60-9
Acide Fmoc-( R , S -3-amino-2-phénylpropionique
Purity:
≥ 98 % (RMN)
Synonym(s):
Acide Fmoc-DL-3-amino-2-phénylpropionique
Documents
$90.00 /250 mg
Taille
Request Bulk Quote
Product Information

Fmoc-(R,S)-3-amino-2-phenylpropionic acid is a versatile amino acid derivative 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 allows for efficient incorporation into peptides, enhancing stability and solubility, making it particularly valuable in the pharmaceutical industry. Researchers often leverage this compound in the development of bioactive peptides and therapeutic agents, where precise amino acid sequences are crucial for efficacy.

The compound's ability to facilitate solid-phase peptide synthesis (SPPS) is a significant advantage, allowing for streamlined processes and higher yields. Furthermore, its application extends to the synthesis of complex natural products and the development of novel drug candidates. With its robust performance in various synthetic pathways, Fmoc-(R,S)-3-amino-2-phenylpropionic acid stands out as a critical building block for researchers aiming to innovate in peptide chemistry and drug formulation.

Synonyms
Acide Fmoc-DL-3-amino-2-phénylpropionique
CAS Number
683217-60-9
Purity
≥ 98 % (RMN)
Molecular Formula
C 24 H 214
Molecular Weight
387.43
MDL Number
MFCD03003582
PubChem ID
2756170
Appearance
Blanc cassé uni
Conditions
Conserver à 0-8°C
General Information
Synonyms
Acide Fmoc-DL-3-amino-2-phénylpropionique
CAS Number
683217-60-9
Purity
≥ 98 % (RMN)
Molecular Formula
C 24 H 214
Molecular Weight
387.43
MDL Number
MFCD03003582
PubChem ID
2756170
Appearance
Blanc cassé uni
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-(R,S)-3-amino-2-phenylpropionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing researchers to selectively modify amino acids without affecting others. Its stability under various conditions makes it a preferred choice in organic chemistry.
  • Drug Development: In pharmaceutical research, this chemical is used to create novel peptide-based drugs. Its unique structure can enhance the bioactivity and specificity of drug candidates, making it valuable in medicinal chemistry.
  • Bioconjugation: The compound is employed in bioconjugation processes, where it helps in attaching biomolecules to surfaces or other molecules. This application is crucial in developing biosensors and targeted drug delivery systems.
  • Research in Neuroscience: Its analogs are studied for their potential effects on neurotransmitter systems, contributing to the understanding of neurological disorders and the development of therapeutic agents.
  • Material Science: This chemical is also explored in the creation of functionalized polymers and materials, which can be used in various applications, including coatings and drug delivery systems, due to their enhanced properties.

Citations