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Catalog Number:
07416
CAS Number:
186320-06-9
Fmoc-β-(3-tienil)-L-alanina
Purity:
≥ 98% (ensayo)
Synonym(s):
Fmoc-L-Ala-3-(3-tienil)-OH, ( S )- N -Fmoc-3-tienilalanina
Documents
$175.96 /1G
Tamaño
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Product Information

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

The compound's distinct structure not only aids in the formation of peptides but also opens avenues for applications in medicinal chemistry, particularly in the design of inhibitors and modulators for various biological targets. Its ability to enhance solubility and stability makes it a preferred choice in pharmaceutical formulations. Researchers can leverage Fmoc-b-(3-thienyl)-L-alanine to explore innovative pathways in drug discovery, particularly in the development of compounds targeting specific diseases, thus expanding the potential for therapeutic interventions.

Synonyms
Fmoc-L-Ala-3-(3-tienil)-OH, ( S )- N -Fmoc-3-tienilalanina
CAS Number
186320-06-9
Purity
≥ 98% (ensayo)
Molecular Formula
C22H19NO4S
Molecular Weight
393.4
MDL Number
MFCD00151916
PubChem ID
4682183
Melting Point
176 - 182 °C (Literatura)
Appearance
Sólido/polvo de color blanco pálido a blanco
Optical Rotation
[a] D 20 = -31 ± 3 ° (C = 1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-Ala-3-(3-tienil)-OH, ( S )- N -Fmoc-3-tienilalanina
CAS Number
186320-06-9
Purity
≥ 98% (ensayo)
Molecular Formula
C22H19NO4S
Molecular Weight
393.4
MDL Number
MFCD00151916
PubChem ID
4682183
Melting Point
176 - 182 °C (Literatura)
Appearance
Sólido/polvo de color blanco pálido a blanco
Optical Rotation
[a] D 20 = -31 ± 3 ° (C = 1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, enhancing the stability and efficiency of the process. Its ability to be easily removed under mild conditions makes it a preferred choice among chemists.
  • Drug Development: Researchers leverage this compound in the design of novel pharmaceuticals, particularly in creating compounds that target specific biological pathways, thanks to its unique thiophene structure that can influence biological activity.
  • Bioconjugation: It is used in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other molecules. This is crucial in developing targeted drug delivery systems and diagnostic tools.
  • Material Science: The compound finds applications in the development of advanced materials, including polymers and nanomaterials, where its properties can enhance conductivity or mechanical strength.
  • Research in Neuroscience: Its structural characteristics make it valuable in studies related to neurotransmitter systems, potentially leading to breakthroughs in understanding neurological disorders.

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