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Catalog Number:
39176
CAS Number:
104322-63-6
(2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent]
Purity:
≥ 95% (Assay by titration)
Synonym(s):
(1S)-(+)-(10-Camphorsulfonyl)oxaziridine, (1S)-(+)-2,N-Epoxy-exo-10,2-bornanesultam
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Product Information

The compound (2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine is a highly effective asymmetric oxidizing reagent, renowned for its utility in organic synthesis. This compound is particularly valuable in the field of asymmetric synthesis, where it facilitates the formation of chiral centers in various organic molecules. Its unique structure allows for selective oxidation reactions, making it an essential tool for chemists aiming to produce enantiomerically pure compounds. This capability is especially beneficial in pharmaceutical development, where the chirality of a compound can significantly influence its biological activity and therapeutic efficacy.

Researchers and industry professionals can leverage (2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine in the synthesis of complex natural products and in the preparation of intermediates for drug development. Its efficiency in promoting oxidation reactions under mild conditions sets it apart from other oxidizing agents, reducing the need for harsh reagents and minimizing by-product formation. This not only streamlines the synthesis process but also enhances the overall yield and purity of the desired products, making it a preferred choice for those in the fields of organic chemistry and medicinal chemistry.

Synonyms
(1S)-(+)-(10-Camphorsulfonyl)oxaziridine, (1S)-(+)-2,N-Epoxy-exo-10,2-bornanesultam
CAS Number
104322-63-6
Purity
≥ 95% (Assay by titration)
Molecular Formula
C10H15NO3S
Molecular Weight
229.29
MDL Number
MFCD00075319
PubChem ID
572659
Melting Point
167 °C
Appearance
White to off-white crystalline powder
Optical Rotation
[α]20D = 47 - 52 ° (C = 1 in Acetone)
Conditions
Store at 0 - 10 °C
General Information
Synonyms
(1S)-(+)-(10-Camphorsulfonyl)oxaziridine, (1S)-(+)-2,N-Epoxy-exo-10,2-bornanesultam
CAS Number
104322-63-6
Purity
≥ 95% (Assay by titration)
Molecular Formula
C10H15NO3S
Molecular Weight
229.29
MDL Number
MFCD00075319
PubChem ID
572659
Melting Point
167 °C
Appearance
White to off-white crystalline powder
Optical Rotation
[α]20D = 47 - 52 ° (C = 1 in Acetone)
Conditions
Store at 0 - 10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine is widely utilized in research focused on:

  • Asymmetric Synthesis: This compound serves as a powerful oxidizing agent in asymmetric synthesis, allowing chemists to create chiral molecules with high selectivity, which is crucial in pharmaceuticals for developing effective drugs.
  • Organic Chemistry Research: It is employed in various organic chemistry applications, particularly in the oxidation of alcohols to aldehydes or ketones, providing a more efficient and selective alternative to traditional oxidizing agents.
  • Drug Development: In the pharmaceutical industry, it aids in the synthesis of complex molecules, enhancing the efficiency of drug discovery processes by enabling the creation of diverse chemical libraries.
  • Material Science: The compound is used in the development of new materials, particularly in creating polymers with specific properties, which can be tailored for applications in coatings and adhesives.
  • Environmental Chemistry: Its application extends to environmental studies, where it can be utilized in the degradation of pollutants, showcasing its potential in green chemistry initiatives aimed at reducing environmental impact.

Citations