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Catalog Number:
43258
CAS Number:
51071-75-1
Hydrogénosulfate de 2,4,6-triphénylpyrylium
Purity:
≥ 97 % (HPLC)
Hazmat
Documents
$330.29 /1G
Taille
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Informations sur le produit

2,4,6-Triphenylpyrylium hydrogensulfate is a versatile compound known for its unique properties and applications in various fields. This organic salt features a triphenylpyrylium cation, which contributes to its remarkable stability and reactivity. It is widely utilized in organic synthesis, particularly in the development of dyes and pigments due to its vibrant color properties. Researchers have found it beneficial in photochemical studies and as a photosensitizer in various chemical reactions, enhancing the efficiency of light-driven processes. Additionally, its ability to act as a strong electrophile makes it a valuable reagent in the synthesis of complex organic molecules, providing a pathway for the creation of novel compounds in medicinal chemistry and materials science.

The compound's unique structure allows for easy functionalization, making it an attractive choice for chemists looking to explore new synthetic routes. Its applications extend to the fields of photonics and electronics, where it can be used in the development of advanced materials. With its diverse potential uses, 2,4,6-Triphenylpyrylium hydrogensulfate stands out as a significant compound for researchers and industry professionals alike, offering innovative solutions and enhancing the scope of chemical research.

Numéro CAS 
51071-75-1
Formule moléculaire
C23H18O5S
Poids moléculaire 
406.45
Point de fusion 
271 °C
Informations générales
Numéro CAS 
51071-75-1
Formule moléculaire
C23H18O5S
Poids moléculaire 
406.45
Point de fusion 
271 °C
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

2,4,6-Triphenylpyrylium hydrogensulfate is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, facilitating the synthesis of various complex molecules through its ability to act as a strong electrophile.
  • Photochemical Applications: It is employed in photochemical studies due to its unique light-absorbing properties, making it useful in the development of light-sensitive materials and dyes.
  • Fluorescent Probes: Researchers use it as a fluorescent probe in biochemical assays, allowing for the tracking of biological processes with high sensitivity and specificity.
  • Electrochemical Sensors: The compound is utilized in the fabrication of electrochemical sensors, enhancing the detection of various analytes in environmental and clinical settings.
  • Material Science: Its properties make it suitable for applications in material science, particularly in the development of advanced polymers and coatings that require specific optical characteristics.

Citations