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Catalog Number:
02456
CAS Number:
130309-35-2
Fmoc-β-(2-tienil)-L-alanina
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-L-Ala-3-(2-tienil)-OH, Fmoc-3-(2-tienil)-L-alanina
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$51.18 /1G
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Product Information

Fmoc-b-(2-thienyl)-L-alanine is a valuable amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which enhances its stability and solubility, making it an ideal choice for solid-phase peptide synthesis. Its unique thiophene side chain not only contributes to the compound's distinct properties but also allows for the incorporation of heterocyclic structures in peptides, which can improve biological activity and selectivity. Researchers and industry professionals appreciate its role in the development of novel therapeutics, particularly in the fields of oncology and neurology, where peptide-based drugs are gaining traction.

In addition to its applications in drug discovery, Fmoc-b-(2-thienyl)-L-alanine serves as a versatile building block in the synthesis of complex biomolecules. Its ability to facilitate the formation of diverse peptide sequences enables chemists to explore a wide range of biological interactions and therapeutic potentials. The compound's favorable characteristics, including its ease of handling and compatibility with various coupling reagents, make it a preferred choice for researchers aiming to innovate in peptide chemistry.

Synonyms
Fmoc-L-Ala-3-(2-tienil)-OH, Fmoc-3-(2-tienil)-L-alanina
CAS Number
130309-35-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H19NO4S
Molecular Weight
393.4
MDL Number
MFCD00065676
PubChem ID
7017915
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-Ala-3-(2-tienil)-OH, Fmoc-3-(2-tienil)-L-alanina
CAS Number
130309-35-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H19NO4S
Molecular Weight
393.4
MDL Number
MFCD00065676
PubChem ID
7017915
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 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-b-(2-thienyl)-L-alanine 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), allowing for the creation of complex peptide structures with high purity.
  • Drug Development: Its unique thiophene structure enhances the pharmacological properties of peptides, making it valuable in the design of novel therapeutics, especially in oncology and neurology.
  • Bioconjugation: The compound can be used in bioconjugation techniques to attach peptides to various biomolecules, facilitating the development of targeted drug delivery systems.
  • Research in Protein Engineering: It aids in the study of protein interactions and modifications, providing insights into protein functionality and stability, which is crucial for biotechnological applications.
  • Analytical Chemistry: Fmoc-b-(2-thienyl)-L-alanine can be utilized as a standard in analytical methods, helping researchers to quantify and analyze peptide compositions effectively.

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