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Catalog Number:
14356
CAS Number:
133083-34-8
(R,S)-Fmoc-2-Amino-3-(7-methoxy-4-coumaryl)propionic acid
Purity:
≥ 97% (HPLC)
Documents
$208.31 /25MG
Pack Size Availability Price
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Product Information

(R,S)-Fmoc-2-Amino-3-(7-methoxy-4-coumaryl)propionic acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure, incorporating a coumarin moiety, enhances its photophysical properties, making it an excellent candidate for applications in fluorescence studies and as a potential drug delivery agent. Researchers have found that this compound can facilitate the development of novel therapeutic agents, particularly in the fields of cancer research and biochemistry, due to its ability to interact with biological targets effectively.

The compound's stability and compatibility with various coupling reagents make it a preferred choice for chemists engaged in solid-phase peptide synthesis. Its distinctive properties allow for the creation of complex peptide structures with improved solubility and bioactivity. As a result, (R,S)-Fmoc-2-Amino-3-(7-methoxy-4-coumaryl)propionic acid stands out in the realm of pharmaceutical and biochemical research, offering significant advantages over traditional amino acids in the design of innovative therapeutic solutions.

CAS Number
133083-34-8
Purity
≥ 97% (HPLC)
Molecular Formula
C28H23NO7
Molecular Weight
485.5
MDL Number
MFCD04112691
PubChem ID
2756174
Appearance
White powder
Conditions
Store at 0 - 8 °C
General Information
CAS Number
133083-34-8
Purity
≥ 97% (HPLC)
Molecular Formula
C28H23NO7
Molecular Weight
485.5
MDL Number
MFCD04112691
PubChem ID
2756174
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

(R,S)-Fmoc-2-Amino-3-(7-methoxy-4-coumaryl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups, which is crucial in developing complex biomolecules.
  • Drug Development: Its unique structure makes it valuable in the design of novel pharmaceuticals, particularly in targeting specific biological pathways, enhancing the efficacy of drug candidates.
  • Bioconjugation: The compound is used in bioconjugation processes, linking biomolecules to therapeutic agents, which is essential in creating targeted therapies in cancer treatment.
  • Fluorescent Probes: Due to its coumarin moiety, it can be employed in creating fluorescent probes for imaging applications in biological research, facilitating the study of cellular processes.
  • Material Science: It finds applications in the development of advanced materials, such as polymers and coatings, where its chemical properties can enhance durability and functionality.

Citations