903570-09-2

Basic information

• Product Name: Benzaldehyde, 4-(methylsulfinyl)-, oxime
• CAS NO: 903570-09-2
• Molecular Formula: C8H9NO2S
• Molecular Weight: 183.231
• Mol File: 903570-09-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 4-(methylsulfinyl)-, oxime(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 4-(methylsulfinyl)-, oxime(903570-09-2)
• EPA Substance Registry System: Benzaldehyde, 4-(methylsulfinyl)-, oxime(903570-09-2)

Safety Data

• Hazardous Substances Data: 903570-09-2(Hazardous Substances Data)

Upstream product

• 93033-60-4 4-(methylthio)benzaldehyde oxime 

Downstream Products

• 1235989-45-3 6,6'-(ethane-1,2-diyl)bis[exo,exo-4,8-epoxy-3a,4,4a,7a,8,8ahexahydro-3-(4-(methylsulfinyl)phenyl)-pyrrolo[3,4-f]-1,2-benzisoxazole-5,7(1H,3aH)-dione] 

Relevant articles and documents

Fe3O4/PEG-SO3H as a heterogeneous and magnetically-recyclable nanocatalyst for the oxidation of sulfides to sulfones or sulfoxides

We present below a sulfonated-polyethylene glycol-coated Fe3O4 nanocomposite (Fe3O4/PEG-SO3H) as a greatly effective and ecological nanocatalyst for the selective oxidation of sulfides to sulfoxides or sulfones with brilliant yields under solvent-free conditions by employing 30% hydrogen peroxide as the oxidant. A number of sulfides containing alcohol, ester, and aldehyde functional groups were fruitfully and selectively oxidized without altering the desired characteristics. The magnetic nanocatalyst (Fe3O4/PEG-SO3H) can be conveniently and swiftly retrieved through the utilization of an external magnetic tool and recycled for more than 10 reaction runs without significantly decreasing its catalytic behavior.

A molybdenum based metallomicellar catalyst for controlled and selective sulfoxidation reactions in aqueous medium

A surfactant based molybdenum system that exhibits catalytic activity for sulfoxidation reactions of various organic sulfides in aqueous medium has been developed and comprehensively characterized using IR, XRD, NMR, ESI-MS, DLS and TEM. The catalyst showcases remarkable selectivity for the preparation of both sulfoxides and sulfones in the range of good to excellent yields. Furthermore, the catalyst showed a high degree of tolerance towards various sensitive functional groups such as hydroxyl, acetal, aldehyde, amine, imine, oxime, cyano and alkene. the Partner Organisations 2014.