70398-91-3

Basic information

• Product Name: Benzene, 1-[(1-methylethyl)thio]-4-(methylthio)-
• CAS NO: 70398-91-3
• Molecular Formula: C10H14S2
• Molecular Weight: 198.353
• Mol File: 70398-91-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 1-[(1-methylethyl)thio]-4-(methylthio)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-[(1-methylethyl)thio]-4-(methylthio)-(70398-91-3)
• EPA Substance Registry System: Benzene, 1-[(1-methylethyl)thio]-4-(methylthio)-(70398-91-3)

Safety Data

• Hazardous Substances Data: 70398-91-3(Hazardous Substances Data)

Upstream product

• 70398-92-4 4-(Ethylthio)-phenyl isopropyl sulphide 
• 74-88-4 methyl iodide 
• 7205-62-1 1-chloro-4-(isopropylthio)benzene 
• 83500-75-8 1-(ethylthio)-4-(methylthio)benzene 
• 699-20-7 1,4-Bis(methylthio)benzene 
• 76227-90-2 p-(Isopropylthio)-thiophenol 
• 5188-07-8 sodium thiomethoxide 
• 75-30-9 2-iodo-propane 
• 1122-97-0 4-methylsulfanyl-thiophenol 
• 106-46-7 para-dichlorobenzene 
• 86636-07-9 p-(methylthio)phenyl benzyl sulphide 
• 17661-83-5 1,4-Bis(ethylthio)benzene 
• 56056-57-6 4-(Ethylthio)-thiophenol 

Downstream Products

• 14905-81-8 1-(isopropylthio)-4-methylbenzene 
• 70398-92-4 4-(Ethylthio)-phenyl isopropyl sulphide 
• 83500-75-8 1-(ethylthio)-4-(methylthio)benzene 
• 3019-20-3 isopropylthiobenzene 
• 85109-97-3 p-(allyl)phenyl i-propyl sulphide 
• 83514-65-2 1-Ethanesulfonyl-4-methanesulfonyl-benzene 
• 85109-98-4 1-allyl-4-(prop-1-en-2-yl)benzene 
• 20120-35-8 4-allylbiphenyl 
• 70399-05-2 1-Methanesulfonyl-4-(propane-2-sulfonyl)-benzene 
• 76227-90-2 p-(Isopropylthio)-thiophenol 
• 1122-97-0 4-methylsulfanyl-thiophenol 
• 92-94-4 [1,1';4',1'']terphenyl 
• 19813-76-4 4-phenylthioanisole 
• 85109-90-6 4-(isopropylthio)biphenyl 

Relevant articles and documents

Simple Syntheses of Aryl Alkyl Thioethers and of Aromatic Thiols from Unactivated Aryl Halides and Efficient Methods for Selective Dealkylation of Aryl Alkyl Ethers and Thioethers

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Reactions of Polychlorobenzenes with Alkanethiol Anions in HMPA. A Simple, High-Yield Synthesis of Poly(alkylthio)benzenes

Reactions of the isomeric trichlorobenzenes and tetrachlorobenzenes and of pentachloro- and hexachlorobenzene with an excess of the sodium salt of the isopropanethiol, in HMPA, afforded the products of complete displacement of all the chlorine atoms present in the molecule.Similar substitutions were also obtained with EtSNa.The reactions with MeSNa were in some cases complicated by the competitive nucleophilic attack at the methyl group of the initially formed aryl methyl thioethers which are thus demethylated to afford thiophenols.