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Catalog Number:
39568
CAS Number:
31571-14-9
anti-(1R)-(+)-Camphorquinone 3-oxime
Purity:
≥ 95% (GC)
Synonym(s):
anti-(1R)-(+)-2,3-Bornanedione 3-oxime
Documents
$162.94 /1G
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Product Information

anti-(1R)-(+)-Camphorquinone 3-oxime is a versatile compound recognized for its unique properties and applications in various fields. This compound, a derivative of camphor, exhibits significant potential in organic synthesis, particularly in the development of fine chemicals and pharmaceuticals. Its structure allows for effective use as a reagent in the synthesis of complex organic molecules, making it invaluable for researchers and industry professionals engaged in chemical research and development. Additionally, its oxime functional group enhances its reactivity, facilitating various transformations that are crucial in synthetic pathways.

In the pharmaceutical industry, anti-(1R)-(+)-Camphorquinone 3-oxime serves as a key intermediate in the synthesis of bioactive compounds, contributing to the development of new therapeutic agents. Its ability to participate in diverse chemical reactions, such as cycloadditions and rearrangements, positions it as a valuable tool for chemists seeking to innovate and optimize synthetic routes. With its favorable properties and practical applications, this compound stands out as an essential resource for advancing research and product development in chemistry.

Synonyms
anti-(1R)-(+)-2,3-Bornanedione 3-oxime
CAS Number
31571-14-9
Purity
≥ 95% (GC)
Molecular Formula
C10H15NO2
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 2 - 8 °C
General Information
Synonyms
anti-(1R)-(+)-2,3-Bornanedione 3-oxime
CAS Number
31571-14-9
Purity
≥ 95% (GC)
Molecular Formula
C10H15NO2
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 2 - 8 °C
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, enabling chemists to create complex structures efficiently.
  • Photochemistry: It is employed in photochemical studies due to its unique light-absorbing properties, making it valuable for researchers exploring light-induced reactions.
  • Pharmaceutical Development: The compound is investigated for its potential applications in drug formulation, particularly in designing new therapeutic agents with improved efficacy.
  • Material Science: Its properties are harnessed in the development of advanced materials, such as polymers and coatings, which require specific chemical characteristics for enhanced performance.
  • Analytical Chemistry: This chemical is used as a standard in various analytical techniques, aiding in the accurate quantification and identification of other compounds in complex mixtures.

Citations