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Catalog Number:
15703
CAS Number:
511272-46-1
Fmoc-(R-3-amino-3-(3-thienyl)propionic acid
Synonym(s):
Fmoc-L-β-Ala-(3-thienyl)-OH, (R-Fmoc-3-thienyl-β-phenylalanine
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Product Information

Fmoc-(R)-3-amino-3-(3-thienyl)propionic 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, incorporating a thiophene ring, enhances its potential for creating bioactive peptides with improved pharmacological properties. Researchers in medicinal chemistry and biochemistry can leverage this compound to develop novel therapeutic agents, particularly in the fields of oncology and neurology, where peptide-based drugs are gaining traction.

The compound's stability and ease of use make it an attractive choice for both academic and industrial applications. Its ability to facilitate the formation of complex peptide structures allows for the exploration of new drug candidates with tailored properties. Additionally, Fmoc-(R)-3-amino-3-(3-thienyl)propionic acid can serve as a building block in the design of peptide libraries, enabling high-throughput screening for potential drug leads. With its promising applications and unique features, this compound is an essential tool for researchers aiming to innovate in peptide chemistry.

Synonyms
Fmoc-L-β-Ala-(3-thienyl)-OH, (R-Fmoc-3-thienyl-β-phenylalanine
CAS Number
511272-46-1
Molecular Formula
C22H19NO4S
Molecular Weight
393.46
MDL Number
MFCD03428027
PubChem ID
24902260
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-L-β-Ala-(3-thienyl)-OH, (R-Fmoc-3-thienyl-β-phenylalanine
CAS Number
511272-46-1
Molecular Formula
C22H19NO4S
Molecular Weight
393.46
MDL Number
MFCD03428027
PubChem ID
24902260
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-3-(3-thienyl)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. Its Fmoc protecting group allows for easy removal during the synthesis process, making it a preferred choice for researchers.
  • Drug Development: The compound's unique thienyl structure can enhance the biological activity of peptides, making it valuable in the pharmaceutical industry for developing new drugs targeting specific diseases.
  • Bioconjugation: It is used in bioconjugation techniques to attach peptides to various biomolecules, facilitating the creation of targeted therapies and diagnostic tools in biomedicine.
  • Research in Neuroscience: The compound's structural properties are beneficial in studying neurotransmitter systems, potentially leading to advancements in treatments for neurological disorders.
  • Material Science: Its application extends to the development of novel materials, where it can be incorporated into polymers or coatings, enhancing their properties for specific industrial uses.

Citations