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Catalog Number:
43159
CAS Number:
60078-97-9
1-Phényl-3-(2,4,6-triméthylphényl)-2-pyrazoline
Purity:
≥ 98% (CG)
Synonym(s):
3-mésityl-1-phényl-2-pyrazoline
Documents
$75.91 /1G
Taille
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Informations sur le produit

1-Phenyl-3-(2,4,6-trimethylphenyl)-2-pyrazoline is a versatile compound known for its unique chemical structure and properties, making it valuable in various applications. This compound exhibits excellent photostability and fluorescence, which are essential characteristics for its use in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices. Its ability to act as a dye or a fluorescent marker allows researchers to utilize it in biological imaging and diagnostics, enhancing visibility and accuracy in experimental setups.

Additionally, 1-Phenyl-3-(2,4,6-trimethylphenyl)-2-pyrazoline has shown potential in the field of materials science, particularly in the synthesis of advanced polymers and coatings that require enhanced thermal and chemical stability. Its unique properties make it a preferred choice for professionals seeking reliable and efficient solutions in their research and industrial applications. With its broad range of uses, this compound stands out as a key ingredient for innovation in various scientific fields.

Numéro CAS 
60078-97-9
Formule moléculaire
C 18 H 20 N 2
Poids moléculaire 
264.37
Point de fusion 
95 - 99 °C
Informations générales
Numéro CAS 
60078-97-9
Formule moléculaire
C 18 H 20 N 2
Poids moléculaire 
264.37
Point de fusion 
95 - 99 °C
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

1-Phenyl-3-(2,4,6-trimethylphenyl)-2-pyrazoline is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile intermediate in the synthesis of various organic molecules, facilitating the development of new pharmaceuticals and agrochemicals.
  • Photochemical Applications: Its unique structure allows it to act as a photosensitizer, making it valuable in photochemical reactions and applications in solar energy conversion.
  • Fluorescent Dyes: The compound is used in the production of fluorescent dyes, which are essential in biological imaging and diagnostics, enhancing visibility in research and clinical settings.
  • Material Science: It contributes to the development of advanced materials, including polymers and coatings, that require specific optical properties for applications in electronics and optics.
  • Biological Research: Researchers utilize this compound in studies related to cell signaling and molecular interactions, providing insights into biological processes and potential therapeutic targets.

Citations