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Catalog Number:
39181
CAS Number:
31571-14-9
anti-(1R-(+)-Camphorquinone 3-oxime
Purity:
≥ 95% (GC)(N)
Synonym(s):
anti-(1R-(+)-2,3-Bornanedione 3-oxime, (1R,E-(+)-Camphorquinone 3-oxime
Documents
$162.94 /1G
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Product Information

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.

Synonyms
anti-(1R-(+)-2,3-Bornanedione 3-oxime, (1R,E-(+)-Camphorquinone 3-oxime
CAS Number
31571-14-9
Purity
≥ 95% (GC)(N)
Molecular Formula
≥ 95% (GC)(N)
Molecular Weight
181.24
MDL Number
MFCD00074848
PubChem ID
6844721
Melting Point
153 - 157 °C
Appearance
White, orange or green crystalline powder
Optical Rotation
[α]20D = 195 - 201 ° (C = 1 in EtOH)
Conditions
Store at RT
General Information
Synonyms
anti-(1R-(+)-2,3-Bornanedione 3-oxime, (1R,E-(+)-Camphorquinone 3-oxime
CAS Number
31571-14-9
Purity
≥ 95% (GC)(N)
Molecular Formula
≥ 95% (GC)(N)
Molecular Weight
181.24
MDL Number
MFCD00074848
PubChem ID
6844721
Melting Point
153 - 157 °C
Appearance
White, orange or green crystalline powder
Optical Rotation
[α]20D = 195 - 201 ° (C = 1 in EtOH)
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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.

Citations