97361-14-3

Basic information

• Product Name: Ethanone, 1-[4-[(4-methoxyphenyl)thio]phenyl]-
• CAS NO: 97361-14-3
• Molecular Formula: C15H14O2S
• Molecular Weight: 258.341
• Mol File: 97361-14-3.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[4-[(4-methoxyphenyl)thio]phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[4-[(4-methoxyphenyl)thio]phenyl]-(97361-14-3)
• EPA Substance Registry System: Ethanone, 1-[4-[(4-methoxyphenyl)thio]phenyl]-(97361-14-3)

Safety Data

• Hazardous Substances Data: 97361-14-3(Hazardous Substances Data)

Upstream product

• 696-63-9 4-Methoxybenzenethiol 
• 13329-40-3 4-Iodoacetophenone 
• 5633-57-8 1-methoxy-4-(phenylsulfanyl)benzene 
• 75-36-5 acetyl chloride 
• 696-62-8 para-iodoanisole 
• 5335-87-5 4,4'-dimethoxyphenyl disulfide 
• 586-89-0 4-acetyl-benzoic acid 
• 350-47-0 1-(4-acetylphenyl)diazonium tetrafluoroborate 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 99-90-1 para-bromoacetophenone 
• 403-42-9 1-(4-fluorophenyl)ethanone 

Relevant articles and documents

A general and inexpensive protocol for the Cu-catalyzed C-S cross-coupling reaction between aryl halides and thiols

A cost effective and easily available CuI/DABCO catalytic system has been developed for C-S cross-coupling reaction. This method is extremely useful for the thioetherification of aryl and heteroaryl halides providing excellent yields and good chemoselectivity.

Forging C?S(Se) Bonds by Nickel-catalyzed Decarbonylation of Carboxylic Acid and Cleavage of Aryl Dichalcogenides

A nickel-catalyzed decarbonylation of carboxylic acids cross-coupling protocol has been developed for the straightforward C?S(Se) bond formation. This reaction is promoted by a commercially-available, user-friendly, inexpensive, air and moisture-stable nickel precatalyst. Various carboxylic acids and a wide range of aryl dichalcogenide substrates were tolerated in this process which afforded products in good to excellent yields. In addition, the present reaction can be conducted on gram scale in good yield.

Electrochemically Promoted Nickel-Catalyzed Carbon-Sulfur Bond Formation

This work describes a nickel-catalyzed Ullmann-type thiolation of aryl iodidesunder mild electrochemical conditions. The simple undivided cell with graphene/nickel foam electrode setups offers excellent substrate tolerance, affording aryl and alkyl sulfides in good chemical yields. Furthermore, the mechanism for this electrochemical cross-coupling reaction has been investigated by cyclic voltammetry.