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Catalog Number:
39173
CAS Number:
2767-84-2
(1 S )-(+)-Camphorquinone
Purity:
≥ 97% (CG)
Synonym(s):
(1 S )-(+)-2,3-bornanedione, (1 S )-(+)-Bornanedione
Documents
$64.00 /1G
Taille
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Informations sur le produit

(1S)-(+)-Camphorquinone is a versatile compound widely recognized for its applications in organic synthesis and photochemistry. This bicyclic diketone is particularly valued in the field of polymer chemistry, where it serves as a photoinitiator in UV-curable coatings and inks, enabling rapid curing processes that enhance production efficiency. Its unique structure allows for effective energy transfer, making it an essential component in the formulation of high-performance materials. Additionally, (1S)-(+)-Camphorquinone is utilized in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals, due to its ability to facilitate reactions such as Michael additions and Diels-Alder reactions.

Researchers and industry professionals appreciate (1S)-(+)-Camphorquinone for its stability and reactivity, which provide significant advantages over similar compounds. Its application in the development of advanced materials and its role in enhancing the efficiency of chemical reactions make it a valuable asset in laboratories and manufacturing settings. With its proven track record in diverse applications, (1S)-(+)-Camphorquinone continues to be a preferred choice for those seeking reliable and effective solutions in their chemical processes.

Numéro CAS 
2767-84-2
Formule moléculaire
C10H14O2
Poids moléculaire 
166.22
Point de fusion 
198 - 202 °C
Rotation optique 
[α] 20 D = 95 - 103 ° (C = 1 dans le toluène)
Informations générales
Numéro CAS 
2767-84-2
Formule moléculaire
C10H14O2
Poids moléculaire 
166.22
Point de fusion 
198 - 202 °C
Rotation optique 
[α] 20 D = 95 - 103 ° (C = 1 dans le toluène)
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

(1S)-(+)-Camphorquinone is widely utilized in research focused on:

  • Photoinitiators in Polymer Chemistry: This compound serves as an effective photoinitiator in UV-curable coatings and inks, enhancing the curing process and improving the durability of the final products.
  • Organic Synthesis: It is employed in various organic synthesis reactions, particularly in the formation of complex molecules, making it a valuable tool for chemists in pharmaceuticals and agrochemicals.
  • Biological Research: Researchers use camphorquinone in studies related to oxidative stress and cell signaling, providing insights into cellular mechanisms and potential therapeutic targets.
  • Dental Applications: In dentistry, it is utilized in light-cured dental materials, improving the bonding and longevity of dental restorations, which is crucial for patient care.
  • Cosmetic Formulations: The compound is also found in cosmetic products for its antioxidant properties, helping to stabilize formulations and enhance skin benefits.

Citations