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Catalog Number:
07417
CAS Number:
220497-90-5
Fmoc-β-(3-thiényl)-D-alanine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-D-Ala-3-(3-thiényl)-OH, ( R )- N -Fmoc-3-thiénylalanine
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$160.00 /1G
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Product Information

Fmoc-b-(3-thienyl)-D-alanine 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 solid-phase peptide synthesis. Its unique thiophene side chain enhances the compound's electronic properties, making it a valuable building block for the design of bioactive peptides and pharmaceuticals. Researchers appreciate its ability to facilitate the creation of peptides with improved stability and bioavailability, which is crucial in the development of therapeutic agents.

In addition to its applications in peptide synthesis, Fmoc-b-(3-thienyl)-D-alanine is also explored in the field of materials science, particularly in the development of organic semiconductors and sensors. Its distinctive structural features allow for the tuning of electronic properties, making it suitable for innovative applications in organic electronics. This compound stands out due to its dual functionality in both biological and material sciences, providing researchers with a powerful tool for advancing their work in diverse fields.

Synonyms
Fmoc-D-Ala-3-(3-thiényl)-OH, ( R )- N -Fmoc-3-thiénylalanine
CAS Number
220497-90-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C 22 H 19 NON 4 S
Molecular Weight
393.4
MDL Number
MFCD00151915
PubChem ID
4682183
Melting Point
184 - 186 °C (lit.)
Appearance
Solide blanc pâle
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-D-Ala-3-(3-thiényl)-OH, ( R )- N -Fmoc-3-thiénylalanine
CAS Number
220497-90-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C 22 H 19 NON 4 S
Molecular Weight
393.4
MDL Number
MFCD00151915
PubChem ID
4682183
Melting Point
184 - 186 °C (lit.)
Appearance
Solide blanc pâle
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-b-(3-thienyl)-D-alanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure makes it valuable in the design of novel pharmaceuticals, particularly in targeting specific biological pathways due to its thiophene moiety.
  • Bioconjugation: The compound can be used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in creating targeted drug delivery systems.
  • Research in Neuroscience: Studies have shown that derivatives of this compound can influence neurotransmitter systems, making it a candidate for research into neurological disorders.
  • Material Science: Its properties can be exploited in the development of new materials, particularly in organic electronics and sensors, due to its conductive characteristics.

Citations