42153-74-2

Basic information

• Product Name: S-Methyl-S-phenyl-N-(p-toluenesulfonyl)sulfoximine
• Synonyms: S-Methyl-S-phenyl-N-(p-toluenesulfonyl)sulfoximine
• CAS NO: 42153-74-2
• Molecular Weight: 309.41
• Mol File: 42153-74-2.mol
• Article Data: 24

Chemical Properties

• CAS DataBase Reference: S-Methyl-S-phenyl-N-(p-toluenesulfonyl)sulfoximine(CAS DataBase Reference)
• NIST Chemistry Reference: S-Methyl-S-phenyl-N-(p-toluenesulfonyl)sulfoximine(42153-74-2)
• EPA Substance Registry System: S-Methyl-S-phenyl-N-(p-toluenesulfonyl)sulfoximine(42153-74-2)

Safety Data

• Hazardous Substances Data: 42153-74-2(Hazardous Substances Data)

Upstream product

• 1193-82-4 racemic methyl phenyl sulfoxide 
• 13150-76-0 N-[(4-methylphenyl)sulfonyl]-S,S-diphenyl-sulfilimine 
• 24702-37-2 C₂₀H₁₉NO₂S₂ 
• 24702-38-3 C₁₉H₁₆ClNO₂S₂ 
• 24698-06-4 S-p-nitrophenyl-S-phenyl-N-tosylsulfilimine 
• 10330-22-0 S-methyl-S-phenyl-N-(p-tolylsulfonyl)sulfilimine 
• 70-55-3 toluene-4-sulfonamide 
• 100-68-5 methyl-phenyl-thioether 
• 1338062-05-7 4-methyl-N-[(2-propoxyphenyl)-λ³-iodanylidene]benzenesulfonamide 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 4381-25-3 (S)-S-methyl-S-phenylsulfoximine 
• 98-59-9 p-toluenesulfonyl chloride 
• 4381-25-3 S-methyl-S-phenylsulfoximine 
• 824-79-3 sodium 4-methylbenzenesulfinate 

Downstream Products

• 82753-99-9 C₁₄H₁₂Br₃NO₃S₂ 
• 82753-94-4 C₁₄H₁₂Cl₃NO₃S₂ 
• 104449-90-3 C₁₄H₁₄INO₃S₂ 
• 1025877-31-9 C₁₇H₂₁NO₆S₃ 
• 147297-64-1 S-<(E)-Pent-1-enyl>-S-phenyl-N-(p-tolylsulfonyl)sulfoximine 
• 110814-66-9 S-(2-Methoxy-2-oxoethyl)-S-phenyl-N-(p-tolylsulfonyl)sulfoximine 
• 139371-79-2 (+)-(S_S)-S-<(1Z,7E)-1,7,9-decatrienyl>-S-phenyl-N-(p-tolylsulphonyl)sulphoximine 
• 142034-15-9 (+)-(S_S)-S-<(1E,7E)-1,7,9-decatrienyl>-S-phenyl-N-(p-tolylsulphonyl)sulphoximine 
• 180720-13-2 (S)-1-(N-tosyl-S-phenylsulfonimidoyl)methylcyclohexanol 
• 180720-12-1 (S)-1-(N-tosyl-S-phenylsulfonimidoyl)methylcyclopentanol 

Relevant articles and documents

I2-Catalyzed N-Sulfonylation of Sulfoximines with Sulfinates in Water at Room Temperature

An oxidative coupling of NH-sulfoximines and arylsulfinates catalyzed by of I2 and H2O2 affords N-sulfonyl sulfoximines. The reaction proceeds under aerobic conditions in water at room temperature. The merits of this proto

Synthetic method of N-aryl sulfone sulfoximine

Sulfoximines have a wide range of applications in organic chemistry, medicinal chemistry, agricultural chemistry, sulfimides are related to the medicinal activity of various organisms, such as antiarrhythmic, antispasmodic, antiasthmatic and antiviral act

O-alkoxyphenyliminoiodanes: Highly efficient reagents for the catalytic aziridination of alkenes and the metal-free amination of organic substrates

Efficient nitrene precursors: Highly reactive iminoiodane-based nitrene precursors were prepared from ortho-alkoxyiodobenzenes. Owing to the presence of the ortho-substituent on the phenyl ring, these new iminoiodanes have excellent solubility in organic