122831-40-7

Basic information

• Product Name: Ethanone, 1-(4-fluorophenyl)-2-(methylthio)-
• CAS NO: 122831-40-7
• Molecular Formula: C9H9FOS
• Molecular Weight: 184.234
• Mol File: 122831-40-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(4-fluorophenyl)-2-(methylthio)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(4-fluorophenyl)-2-(methylthio)-(122831-40-7)
• EPA Substance Registry System: Ethanone, 1-(4-fluorophenyl)-2-(methylthio)-(122831-40-7)

Safety Data

• Hazardous Substances Data: 122831-40-7(Hazardous Substances Data)

Upstream product

• 403-29-2 2-bromo-4'-fluoroacetophenone 
• 403-42-9 1-(4-fluorophenyl)ethanone 
• 5188-07-8 sodium thiomethoxide 
• 74-93-1 methylthiol 

Downstream Products

• 82652-17-3 1-(4-fluorophenyl)-2-(methylsulfonyl)-1-ethanone 
• 192862-13-8 2,2-Difluoro-1-(4-fluorophenyl)-2-(methylthio)-1-ethanone 
• 1292821-93-2 C₂₆H₂₃FN₂O₂S 
• 192861-87-3 1,1-difluoro-2-(4-fluorophenyl)-1-(methylthio)-3-(1H-1,2,4-triazol-1-yl)-2-propanol 
• 192862-18-3 2-[difluoro(methylthio)methyl]-2-(4-fluorophenyl)oxirane 

Relevant articles and documents

SUBSTITUTED NAPHTHYRIDINONE COMPOUNDS USEFUL AS T CELL ACTIVATORS

Disclosed are compounds of Formula (I) or a salt thereof, wherein: R1, R2, R3, R4, R5, and m are defined herein. Also disclosed are methods of using such compounds to inhibit the activity of one or both of diacylglycerol kinase alpha (DGKα) and diacylglycerol kinase zeta (DGKζ), and pharmaceutical compositions comprising such compounds. These compounds are useful in the treatment of viral infections and proliferative disorders, such as cancer.

Rh/DuanPhos-Catalyzed Asymmetric Hydrogenation of β-Acetylamino Vinylsulfides: An Approach to Chiral β-Acetylamino Sulfides

Rh/DuanPhos-catalyzed asymmetric hydrogenation of challenging β-acetylamino vinylsulfides has been developed, affording chiral β-acetylamino sulfides with high yields and excellent ee's (up to 99% ee). This novel methodology provides an efficient and concise synthetic route to chiral β-acetylamino sulfides. The potential utility of this protocol in the synthesis of Apremilast has also been disclosed.