127411-75-0

Basic information

• Product Name: (1S)-(+)-CAMPHORLACTONE-SULFONYLOXAZIRIDINE
• Synonyms: (1S)-(+)-CAMPHORLACTONE-SULFONYLOXAZIRIDINE;5H-4a,7-Methano-4H,9H-oxazirino2,3-boxepino3,4-cisothiazol-9-one, dihydro-10,10-dimethyl-, 2,2-dioxide, 4aS-(4a.alpha.,7.alpha.,9aS*)-;(1S)-(+)-CAMPHORLACTONE-SULFONYLOXAZIRIDINE 98+%;(1S)-(+)-CAMPHORLACTONE-SULFONYLOXAZIRID
• CAS NO: 127411-75-0
• Molecular Formula: C10H13NO5S
• Molecular Weight: 259.28
• Mol File: 127411-75-0.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (1S)-(+)-CAMPHORLACTONE-SULFONYLOXAZIRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: (1S)-(+)-CAMPHORLACTONE-SULFONYLOXAZIRIDINE(127411-75-0)
• EPA Substance Registry System: (1S)-(+)-CAMPHORLACTONE-SULFONYLOXAZIRIDINE(127411-75-0)

Safety Data

• Hazardous Substances Data: 127411-75-0(Hazardous Substances Data)

Usage

Description

(1S)-(+)-CAMPHORLACTONE-SULFONYLOXAZIRIDINE is a unique compound that integrates the structure of camphor with a sulfonyloxaziridine functional group. This combination endows the molecule with distinctive properties that are valuable in various chemical processes.
Used in Organic Synthesis:
(1S)-(+)-CAMPHORLACTONE-SULFONYLOXAZIRIDINE is used as a chiral reagent for the asymmetric epoxidation of olefins. Its chiral nature allows for the formation of enantiopure products, which is crucial in the synthesis of chiral molecules that are essential in pharmaceutical and agrochemical industries.
Used in Pharmaceutical Industry:
(1S)-(+)-CAMPHORLACTONE-SULFONYLOXAZIRIDINE is used as a building block in the preparation of various pharmaceutical compounds. Its high reactivity and selectivity in oxidation reactions make it a valuable tool in the synthesis of complex organic molecules with specific biological activities.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, (1S)-(+)-CAMPHORLACTONE-SULFONYLOXAZIRIDINE is utilized as a key component in the synthesis of agrochemical compounds. Its ability to facilitate the creation of enantiopure products ensures the development of effective and targeted agrochemicals with minimal environmental impact.