3406-65-3

Basic information

• Product Name: E-4-methoxystyryl 4-chlorophenyl sulfone
• Synonyms: E-4-methoxystyryl 4-chlorophenyl sulfone
• CAS NO: 3406-65-3
• Molecular Weight: 308.785
• Mol File: 3406-65-3.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: E-4-methoxystyryl 4-chlorophenyl sulfone(CAS DataBase Reference)
• NIST Chemistry Reference: E-4-methoxystyryl 4-chlorophenyl sulfone(3406-65-3)
• EPA Substance Registry System: E-4-methoxystyryl 4-chlorophenyl sulfone(3406-65-3)

Safety Data

• Hazardous Substances Data: 3406-65-3(Hazardous Substances Data)

Upstream product

• 14752-66-0 sodium p-chlorobenzenesulphinate 
• 768-60-5 4-methoxyphenylacetylen 
• 637-69-4 4-Methoxystyrene 
• 98-60-2 4-chlorobenzenesulfonyl chloride 
• 2751-25-9 p-chlorophenylsulfonyl hydrazide 
• 3179-10-0 1-methoxy-4-(2-nitro-vinyl)-benzene 
• 943-89-5 (E)-3-(4-methoxyphenyl)acrylic acid 
• 69770-58-7 diethyl<<(p-chlorophenyl)sulfide>methyl>phosphonate 
• 3405-89-8 2-(4-chloro-phenylsulfonyl)acetic acid 
• 123-11-5 4-methoxy-benzaldehyde 
• 1202639-06-2 C₂₈H₂₉ClN₄O₁₁S 
• 106-54-7 p-Chlorothiophenol 
• 3405-88-7 (4-chlorophenylthio)acetic acid 

Downstream Products

• 86432-78-2 C₁₆H₁₅ClO₃S 

Relevant articles and documents

Synthesis of vinyl sulfones through sulfonylation of styrenes with sulfonyl chlorides under metal-free conditions

A hypervalent iodine reagent-mediated sulfonylation of styrenes with sulfonyl chlorides was developed for the synthesis of vinyl sulfones. The reaction proceeded under metal-free, mild and neutral conditions without extra oxidants or bases. It also exhibited good air and moisture tolerance, broad substrate scope and high chemo-selectivity, affording the vinyl sulfones in moderate to good yields.

A Study of Graphene-Based Copper Catalysts: Copper(I) Nanoplatelets for Batch and Continuous-Flow Applications

The use of graphene derivatives as supports improves the properties of heterogeneous catalysts, with graphene oxide (GO) being the most frequently employed. To explore greener possibilities as well as to get some insights into the role of the different gr

Mn(III)-mediated regioselective synthesis of (: E)-vinyl sulfones from sodium sulfinates and nitro-olefins

An efficient Mn(iii)-mediated coupling reaction of sodium sulfinates with nitro-olefins has been developed, this reaction proceeds in mild and open-flask conditions to afford (E)-vinyl sulfones with high regioselectivities and in good to excellent yields. The control experiments revealed that this transformation could involve a radical process.