246224-09-9

Basic information

• Product Name: Benzaldehyde, 3-methoxy-4-[[(4-methylphenyl)sulfonyl]oxy]-
• CAS NO: 246224-09-9
• Molecular Formula: C15H14O5S
• Molecular Weight: 306.339
• Mol File: 246224-09-9.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 3-methoxy-4-[[(4-methylphenyl)sulfonyl]oxy]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 3-methoxy-4-[[(4-methylphenyl)sulfonyl]oxy]-(246224-09-9)
• EPA Substance Registry System: Benzaldehyde, 3-methoxy-4-[[(4-methylphenyl)sulfonyl]oxy]-(246224-09-9)

Safety Data

• Hazardous Substances Data: 246224-09-9(Hazardous Substances Data)

Upstream product

• 74-83-9 methyl bromide 
• 121-33-5 vanillin 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 611235-56-4 4-formyl-2,2'-dimethoxybiphenyl 
• 1614826-41-3 bis(3-methoxy-4-tosylhydroxybenzyl)ether 
• 121-33-5 vanillin 

Relevant articles and documents

Synthesis, characterization, biological activity and molecular docking studies of novel schiff bases derived from thiosemicarbazide: Biochemical and computational approach

In this study, eight new Schiff base derivatives (2a-h) were synthesized and their inhibition activities against Acetylcholinesterase (AChE), Butyrylcholinesterase (BChE), α-Glucosidase and Lactoperoxidase (LPO) were investigated. Structures of the synthe

Synthesis and anticancer activity of novel hydrazone linkage-based aryl sulfonate derivatives as apoptosis inducers

In the present study, the various 28 hybrid molecules containing hydrazone and sulfonate moieties were synthesized and characterized by FTIR, 1H-NMR, 13C-NMR spectroscopy and LC-MS spectrometry, besides elemental analysis. The compou

A Mild and Selective Method for the Catalytic Hydrodeoxygenation of Cyanurate Activated Phenols in Multiphasic Continuous Flow

A low-energy, high-selectivity approach to the catalytic hydrodeoxygenation of phenols is reported using batch or continuous flow methods to react 3 equiv of phenol with cyanuric chloride then hydrogenolyzing the triarylcyanurate intermediate to give 3 equiv of deoxo aromatic. The use of cyanuric chloride compares favorably with existing activation methods, showing improved scalability, atom efficiency, and economics. The scope of both the activation and hydrogenolysis stages are explored using lignin-related phenols. Initial development has identified that continuous stir tank reactors (CSTRs) enable a multiphasic process for converting guaiacol to anisole and at steady state overcome the catalyst deactivation issues observed in batch, seemingly caused by the cyanurate byproduct. Green chemistry aspects and the potential for industrial adoption are discussed.