34602-11-4

Basic information

• Product Name: Benzene, 1-methoxy-2-[[(4-methylphenyl)sulfonyl]methyl]-
• CAS NO: 34602-11-4
• Molecular Formula: C15H16O3S
• Molecular Weight: 276.356
• Mol File: 34602-11-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, 1-methoxy-2-[[(4-methylphenyl)sulfonyl]methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-methoxy-2-[[(4-methylphenyl)sulfonyl]methyl]-(34602-11-4)
• EPA Substance Registry System: Benzene, 1-methoxy-2-[[(4-methylphenyl)sulfonyl]methyl]-(34602-11-4)

Safety Data

• Hazardous Substances Data: 34602-11-4(Hazardous Substances Data)

Upstream product

• 135-02-4 ortho-anisaldehyde 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 138298-13-2 C₁₅H₁₆OS 
• 138298-09-6 1-methoxy-2-[(p-tolylsulfinyl)methyl]benzene 
• 19350-70-0 2-methoxybenzaldehyde p-toluenesulfonylhydrazone 
• 7035-02-1 o-Methoxybenzyl chloride 

Downstream Products

• 77853-46-4 4-(2-Methoxyphenyl)-butanenitrile 
• 33209-75-5 4-(2-Methoxyphenyl)-butanoic acid 
• 33209-76-6 Ethyl 4-(2-Methoxyphenyl)-butanoate 
• 77853-47-5 3-Methoxycarbonyl-1-(2-methoxyphenyl)-propyl-4-tolylsulfone 
• 77853-41-9 α-(2-Cyanoethyl)-2-methoxybenzyl-4-tolylsulfone 

Relevant articles and documents

Iron(III) phthalocyanine-chloride-catalyzed synthesis of sulfones from sulfonylhydrazones

In this study, sulfones are synthesized from sulfonylhydrazones catalyzed by iron(III) phthalocyanine chloride. This reaction offers broad substrate scope, occurs under mild conditions, utilized readily available reactants, and forms products in good-to-h

Kinetic resolution in vanadium-catalyzed sulfur oxidation as an efficient route to enantiopure aryl benzyl sulfoxides

Enantiopure aryl benzyl sulfoxides can be prepared using vanadium-Schiff base catalyzed sulfide oxidation and kinetic resolution of the resulting sulfoxide. The kinetic resolution can be effected in combination with asymmetric sulfide oxidation or instead starting from the racemic sulfoxide. Georg Thieme Verlag Stuttgart.