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Catalog Number:
39180
CAS Number:
104372-31-8
(2S,8aR)-(-)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent]
Purity:
≥ 95% (Assay by titration)
Synonym(s):
(1R)-(-)-(10-Camphorsulfonyl)oxaziridine, (1R)-(-)-2,N-Epoxy-exo-10,2-bornanesultam
Documents
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Product Information

The compound (2S,8aR)-(-)-(Camphorylsulfonyl)oxaziridine is a highly effective asymmetric oxidizing reagent, renowned for its utility in organic synthesis. This compound is particularly valued in the field of asymmetric synthesis, where it facilitates the selective oxidation of various substrates, leading to the formation of chiral alcohols and other functional groups. Its unique structure allows for high regio- and stereoselectivity, making it an essential tool for chemists aiming to produce enantiomerically pure compounds.

Researchers and industry professionals can leverage this compound in the development of pharmaceuticals, agrochemicals, and fine chemicals, where the precise control of stereochemistry is crucial. The ability to achieve high yields with minimal by-products enhances its appeal in both academic research and industrial applications. Additionally, its compatibility with a wide range of functional groups expands its applicability, making it a versatile choice for synthetic chemists.

Synonyms
(1R)-(-)-(10-Camphorsulfonyl)oxaziridine, (1R)-(-)-2,N-Epoxy-exo-10,2-bornanesultam
CAS Number
104372-31-8
Purity
≥ 95% (Assay by titration)
Molecular Formula
C10H15NO3S
Molecular Weight
229.29
MDL Number
MFCD00075428
PubChem ID
572659
Melting Point
168 °C
Appearance
White to off-white crystalline powder
Optical Rotation
[α]20D = -47 to -52 ° (C = 1 in Acetone)
Conditions
Store at 0 - 10 °C
General Information
Synonyms
(1R)-(-)-(10-Camphorsulfonyl)oxaziridine, (1R)-(-)-2,N-Epoxy-exo-10,2-bornanesultam
CAS Number
104372-31-8
Purity
≥ 95% (Assay by titration)
Molecular Formula
C10H15NO3S
Molecular Weight
229.29
MDL Number
MFCD00075428
PubChem ID
572659
Melting Point
168 °C
Appearance
White to off-white crystalline powder
Optical Rotation
[α]20D = -47 to -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

(2S,8aR)-(-)-(Camphorylsulfonyl)oxaziridine is widely utilized in research focused on:

  • Asymmetric Synthesis: This compound serves as a powerful oxidizing reagent in asymmetric synthesis, allowing chemists to create chiral molecules with high selectivity. This is particularly valuable in pharmaceuticals where the chirality of a compound can significantly affect its efficacy and safety.
  • Drug Development: In the pharmaceutical industry, it is used to synthesize complex drug molecules. Its ability to introduce functional groups selectively makes it an essential tool in the development of new medications, improving the efficiency of drug discovery processes.
  • Organic Chemistry Research: Researchers utilize this compound in various organic reactions, including the oxidation of alcohols to carbonyl compounds. This application is crucial for creating intermediates in organic synthesis, enhancing the versatility of synthetic pathways.
  • Material Science: The compound can be employed in the modification of polymers and materials, leading to improved properties such as increased stability and enhanced performance in various applications, including coatings and adhesives.
  • Environmental Chemistry: It plays a role in the development of environmentally friendly oxidation processes, reducing the use of hazardous reagents and minimizing waste, which aligns with the growing demand for sustainable practices in chemical manufacturing.

Citations