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Catalog Number:
04079
CAS Number:
177966-61-9
Fmoc-3-benzotienil-D-alanina
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-3-D-Ala(3-benzotienil)-OH
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$145.90 /1G
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Product Information

Fmoc-3-(3-benzothienyl)-D-alanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique benzothiophene moiety, which enhances its bioactivity and stability, making it an excellent choice for researchers focused on developing novel therapeutic agents. Its Fmoc (9-fluorenylmethyloxycarbonyl) protecting group allows for easy incorporation into peptide chains, facilitating the synthesis of complex peptides with improved pharmacological properties.

In the pharmaceutical industry, Fmoc-3-(3-benzothienyl)-D-alanine is particularly valuable for creating targeted drug delivery systems and studying receptor interactions. Its distinctive structure can lead to the development of peptides with enhanced selectivity and potency, which is crucial in the design of drugs aimed at specific biological targets. Researchers can leverage this compound to explore new avenues in medicinal chemistry and biochemistry, making it an essential addition to any laboratory focused on peptide research and development.

Synonyms
Fmoc-3-D-Ala(3-benzotienil)-OH
CAS Number
177966-61-9
Purity
≥ 97 % (HPLC)
Molecular Formula
C26H21NO4S
Molecular Weight
443.5
MDL Number
MFCD00672563
PubChem ID
4003594
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-3-D-Ala(3-benzotienil)-OH
CAS Number
177966-61-9
Purity
≥ 97 % (HPLC)
Molecular Formula
C26H21NO4S
Molecular Weight
443.5
MDL Number
MFCD00672563
PubChem ID
4003594
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-3-(3-benzothienyl)-D-alanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure can enhance the bioactivity of peptide-based drugs, making it valuable in pharmaceutical research for developing new therapies.
  • Bioconjugation: The compound can be used to create conjugates with biomolecules, facilitating the study of protein interactions and the development of targeted drug delivery systems.
  • Material Science: In materials research, it can be incorporated into polymers to create materials with specific properties, such as increased thermal stability or enhanced electrical conductivity.
  • Fluorescent Probes: The benzothienyl group can be utilized in the design of fluorescent probes for imaging applications, aiding researchers in visualizing cellular processes in real-time.

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