7431-33-6

Upstream product

• 106-44-5 p-cresol 
• 624-92-0 Dimethyldisulphide 
• 60774-07-4 4-methyl-2-mercaptophenol 
• 77-78-1 dimethyl sulfate 
• 83485-33-0 2-methoxy-5-methylbenzenethiol 
• 95-84-1 3-amino-4-hydroxytoluene 
• 7429-90-5 aluminium 

Downstream Products

• 88041-62-7 4-methyl-2-(methylsulfonyl)phenol 
• 15267-50-2 (4-Methyl-2-methylmercapto-phenoxy)-essigsaeuremethylester 
• 15267-51-3 (4-Methyl-2-methylmercapto-phenoxy)-essigsaeure 
• 15267-66-0 (4-Methyl-2-methylmercapto-phenoxy)-acethydroxamsaeure 
• 15267-67-1 (4-Methyl-2-methylmercapto-phenoxy)-essigsaeurehydrazid 
• 949566-81-8 2-[(bis(2-pyridylmethyl)amino)methyl]-4-methyl-6-(methylthio)phenol 
• 1350815-04-1 4-methyl-2-methylthio-1-phenoxybenzene 
• 193804-62-5 1-(2-hydroxy-5-methyl-3-(methylthio)benzyl)-4,7-diisopropyl-1,4,7-triazacyclononane 
• 153046-30-1 2-methylsulfinyl-4-methylphenol 
• 91011-44-8 Methyl-phosphonothioic acid O-methyl ester O-(4-methyl-2-methylsulfanyl-phenyl) ester 

Relevant academic research and scientific papers

Synthetic models of the inactive Copper(II)-tyrosinate and active Copper(II)-tyrosyl radical forms of galactose and glyoxal oxidases

A series of Cu(II) and Zn(II) complexes with new ligands having either one or two substituted phenolates appended to the 1,4,7-triazacyclononane frame were prepared and characterized by optical absorption, EPR, NMR, and/or resonance Raman spectroscopy, cy

Preparation of ortho-(alkyl-or arylthio) phenols

Strong acids, e.g., aluminosilicates and sulfonic acids are employed as catalysts for the (alkyl or aryl)thiolation of phenols using dialkyl or diaryl disulfides and/or (alkyl- or arylthio)phenols as thiolating agents, and for the isomerization of (alkyl- or arylthio)phenols, to prepare ortho--(alkyl- or arylthio)phenols as the predominant products.

Preparation of ortho-(alkyl- or arylthio)phenols

Strong acids, e.g., aluminosilicates and sulfonic acids are employed as catalysts for the (alkyl or aryl)thiolation of phenols using dialkyl or diaryl disulfides and/or (alkyl- or arylthio)phenols as thiolating agents, and for the isomerization of (alkyl- or arylthio)phenols, to prepare ortho(alkyl- or arylthio)phenols as the predominant products.

Process for the preparation of ortho-(hydrocarbylthio)-phenols

Disclosed is a process for the preparation of otho-(hydrocarbylthio)-phenols, having at least one hydrogen on a carbon atom ortho to a hydroxy group, with hydrocarbyl disulfides in the presence of catalytic amounts of aluminum phenoxide.