123559-06-8

Basic information

• Product Name: 4,4-Bis-methylsulfanyl-2-p-tolyl-but-3-en-2-ol
• Synonyms: 4,4-Bis-methylsulfanyl-2-p-tolyl-but-3-en-2-ol
• CAS NO: 123559-06-8
• Molecular Weight: 254.417
• Mol File: 123559-06-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4,4-Bis-methylsulfanyl-2-p-tolyl-but-3-en-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4-Bis-methylsulfanyl-2-p-tolyl-but-3-en-2-ol(123559-06-8)
• EPA Substance Registry System: 4,4-Bis-methylsulfanyl-2-p-tolyl-but-3-en-2-ol(123559-06-8)

Safety Data

• Hazardous Substances Data: 123559-06-8(Hazardous Substances Data)

Upstream product

• 917-64-6 methyl magnesium iodide 
• 41467-27-0 3,3-bis(methylthio)-1-(p-tolyl)prop-2-en-1-one 
• 74-88-4 methyl iodide 

Downstream Products

• 123559-12-6 1,1-bis(methylthio)-3-(4-methylphenyl)-1,3-butadiene 
• 70964-89-5 E-methyl β-methyl-p-methylcinnamate 

Relevant articles and documents

Reactions of α-hydroxyketene dithioacetals with Lawesson's reagent: An efficient method for the synthesis of α,β-unsaturated dithioesters

The α-hydroxyketene dithioacetals 2 and 5, obtained from α-oxoketene dithioacetals by the 1,2-reduction or the 1,2-addition of carbon nucleophiles, on treatment with Lawesson's reagent afforded α,β-unsaturated dithioesters 3 and 6 in good yields. Georg Th

STUDIES ON DIELS-ALDER CYCLOADDITIONS OF VINYLKETENE DITHIOACETALS

The Diels-Alder cycloadditions of the acyclic and cyclic vinylketene dithioacetals 4 prepared from the corresponding oxoketene dithioacetals 2, either by 1,2-addition of methylmagnesium iodide and subsequent dehydration or by Wittig reaction, were studied