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Catalog Number:
15698
CAS Number:
507472-08-4
Fmoc-(S-3-amino-3-(2-thienyl)propionic acid
Synonym(s):
Fmoc-D-β-Ala-(2-thienyl)-OH, (R-Fmoc-2-thienyl-β-phenylalanine
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$250.80 /1G
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Product Information

Fmoc-(S)-3-amino-3-(2-thienyl)propionic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a unique thienyl side chain, which enhances its ability to form stable peptide bonds, making it an ideal choice for researchers focusing on the design of bioactive peptides and pharmaceuticals. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for easy deprotection under mild conditions, facilitating streamlined synthesis processes.

In addition to its applications in academic research, Fmoc-(S)-3-amino-3-(2-thienyl)propionic acid is particularly valuable in the development of peptide-based therapeutics, where the incorporation of thiophene derivatives can improve the pharmacological properties of the resulting compounds. This compound's unique structure not only aids in enhancing solubility and stability but also provides opportunities for creating novel therapeutic agents with improved efficacy. Researchers and industry professionals can leverage this compound to explore innovative solutions in drug discovery and development.

Synonyms
Fmoc-D-β-Ala-(2-thienyl)-OH, (R-Fmoc-2-thienyl-β-phenylalanine
CAS Number
507472-08-4
Molecular Formula
C22H19NO4S
Molecular Weight
393.46
MDL Number
MFCD03427988
PubChem ID
24902259
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-D-β-Ala-(2-thienyl)-OH, (R-Fmoc-2-thienyl-β-phenylalanine
CAS Number
507472-08-4
Molecular Formula
C22H19NO4S
Molecular Weight
393.46
MDL Number
MFCD03427988
PubChem ID
24902259
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-(S)-3-amino-3-(2-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 (SPPS), enhancing the efficiency and yield of desired peptide sequences.
  • Drug Development: Its unique structure allows for the creation of novel therapeutic agents, especially in the development of drugs targeting specific biological pathways, making it valuable in pharmaceutical research.
  • Bioconjugation: The compound is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, aiding in the development of targeted drug delivery systems and diagnostics.
  • Research on Protein Interactions: It plays a role in studying protein-ligand interactions, which is crucial for understanding biological processes and developing new therapeutic strategies.
  • Material Science: The compound can be incorporated into polymers or materials to enhance their properties, such as conductivity or biocompatibility, which is beneficial in various industrial applications.

Citations