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Catalog Number:
39181
CAS Number:
31571-14-9
anti-(1 R -(+)-Canforquinona 3-oxima
Purity:
≥ 95 % (GC)(N)
Synonym(s):
anti -(1 R -(+)-2,3-bornanodiona 3-oxima, (1 R , E -(+)-Canforquinona 3-oxima
Documents
$162.94 /1G
Tamaño
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Información del producto

The compound anti-(1R)-(+)-Camphorquinone 3-oxime is a valuable chemical in various applications, particularly in organic synthesis and as a reagent in analytical chemistry. This compound is recognized for its unique structural properties, which allow it to function effectively as a chiral auxiliary in asymmetric synthesis. Its ability to facilitate the formation of enantiomerically enriched products makes it a preferred choice among researchers and industry professionals working in pharmaceuticals and fine chemicals.

Additionally, anti-(1R)-(+)-Camphorquinone 3-oxime exhibits notable stability and reactivity, which enhances its utility in photochemical reactions and as a precursor in the synthesis of complex organic molecules. Its application in the development of new materials and in the field of medicinal chemistry underscores its significance. The compound's versatility and efficiency in promoting specific reactions make it an essential tool for chemists aiming to innovate and improve synthetic pathways.

Número CAS
31571-14-9
Fórmula molecular
≥ 95 % (GC)(N)
Peso molecular
181.24
Número MDL
MFCD00074848
Punto de fusión
153 - 157 °C
Rotación óptica
[α] 20 D = 195 - 201 ° (C = 1 en EtOH)
Condiciones
Tienda en RT
Información general
Número CAS
31571-14-9
Fórmula molecular
≥ 95 % (GC)(N)
Peso molecular
181.24
Número MDL
MFCD00074848
Punto de fusión
153 - 157 °C
Rotación óptica
[α] 20 D = 195 - 201 ° (C = 1 en EtOH)
Condiciones
Tienda en RT
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

anti-(1R)-(+)-Camphorquinone 3-oxime is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile intermediate in the synthesis of various organic molecules, particularly in the creation of complex natural products and pharmaceuticals.
  • Photochemical Applications: It is used in photochemical reactions, where its unique structure allows for the generation of reactive intermediates, enhancing the efficiency of light-driven processes.
  • Analytical Chemistry: The compound is employed as a reagent in analytical methods, helping to identify and quantify other substances in complex mixtures, which is crucial in quality control in laboratories.
  • Material Science: It finds applications in the development of advanced materials, including polymers and coatings, where its properties can improve durability and performance.
  • Medicinal Chemistry: Researchers utilize this compound in drug discovery, particularly in the design of new therapeutic agents that target specific biological pathways, offering potential advantages over existing treatments.

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