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Catalog Number:
39177
CAS Number:
10334-26-6
(1 R )-(-)-Camphorquinone
Purity:
≥ 98% (CG)
Synonym(s):
(1 R )-(-)-2,3-bornanedione
Documents
$40.96 /1G
Taille
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Informations sur le produit

(1R)-(-)-Camphorquinone is a versatile compound widely utilized in various fields, particularly in organic synthesis and photochemistry. This bicyclic ketone is recognized for its unique ability to act as a photoinitiator, making it invaluable in the production of polymers and resins. Its strong UV absorption properties allow it to initiate polymerization processes effectively, which is crucial in industries such as coatings, adhesives, and dental materials. Additionally, (1R)-(-)-Camphorquinone serves as a key intermediate in the synthesis of complex organic molecules, enhancing its relevance in pharmaceutical research and development.

Researchers appreciate (1R)-(-)-Camphorquinone for its efficiency and effectiveness in various applications, including its role in the development of light-sensitive materials. Its unique structure not only contributes to its reactivity but also provides advantages over similar compounds, such as improved stability and a broader range of applications. This compound is essential for professionals seeking reliable and effective solutions in their chemical processes, making it a valuable addition to any laboratory or industrial setting.

Numéro CAS 
10334-26-6
Formule moléculaire
C10H14O2
Poids moléculaire 
166.22
Point de fusion 
200 - 204 °C
Rotation optique 
[α] 20 D = -95 à -105 ° (C = 1 dans le toluène)
Informations générales
Numéro CAS 
10334-26-6
Formule moléculaire
C10H14O2
Poids moléculaire 
166.22
Point de fusion 
200 - 204 °C
Rotation optique 
[α] 20 D = -95 à -105 ° (C = 1 dans le toluène)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

(1R)-(-)-Camphorquinon is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, enabling the synthesis of complex molecules and facilitating the development of new pharmaceuticals.
  • Photochemistry: It is used in photochemical reactions, particularly in the study of light-induced processes, which can lead to advancements in solar energy applications and materials science.
  • Cosmetic Formulations: Due to its aromatic properties, it is incorporated into cosmetic products for fragrance and as a potential skin conditioning agent, enhancing product appeal.
  • Analytical Chemistry: This compound is employed as a standard in analytical methods, helping researchers accurately measure and analyze various substances in complex mixtures.
  • Biological Research: It plays a role in biological studies, particularly in understanding enzyme mechanisms and interactions, contributing to drug discovery and development.

Citations