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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Oxaziridine, 2-[(4-methylphenyl)sulfonyl]-3-phenyl-

Cc1ccc(cc1)S(=O)(=O)N1OC1c1ccccc1 Request for Quotation
Chemical Name: Oxaziridine, 2-[(4-methylphenyl)sulfonyl]-3-phenyl-
CAS Number: 63160-12-3
Product Number: AG00EKEY(AGN-PC-0NDNNX)
Synonyms:
MDL No:
Molecular Formula: C14H13NO3S
Molecular Weight: 275.3229

Identification/Properties

Properties
MP:
87℃ (decomp)
Storage:
Inert atmosphere;2-8℃;
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Phenyl-2-tosyl-1,2-oxaziridine is a versatile and valuable intermediate in chemical synthesis. This compound is widely utilized in asymmetric epoxidation reactions, where it serves as a chiral source of oxygen atoms, leading to the formation of enantioenriched epoxides. Its unique structure enables selective and efficient epoxidation of a variety of alkenes, providing access to a range of chiral building blocks used in the synthesis of pharmaceuticals, natural products, and functional materials. Additionally, 3-Phenyl-2-tosyl-1,2-oxaziridine can participate in other transformations such as cyclopropanation, aziridination, and C−H functionalization reactions, making it a valuable tool for chemists in the development of complex molecular architectures.