1360171-43-2

Basic information

• Product Name: 2,4-bis(trifluoromethylsulfonyloxy)benzophenone
• Synonyms: 2,4-bis(trifluoromethylsulfonyloxy)benzophenone
• CAS NO: 1360171-43-2
• Molecular Weight: 478.347
• Mol File: 1360171-43-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,4-bis(trifluoromethylsulfonyloxy)benzophenone(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-bis(trifluoromethylsulfonyloxy)benzophenone(1360171-43-2)
• EPA Substance Registry System: 2,4-bis(trifluoromethylsulfonyloxy)benzophenone(1360171-43-2)

Safety Data

• Hazardous Substances Data: 1360171-43-2(Hazardous Substances Data)

Upstream product

• 131-56-6 2.4-dihydroxybenzophenone 
• 358-23-6 trifluoromethylsulfonic anhydride 

Downstream Products

• 1360171-68-1 [2,4-di(dec-1-ynyl)phenyl]phenylmethanone 
• 1360171-70-5 2-benzoyl-5-(dec-1-ynyl)phenyl trifluoromethanesulfonate 
• 1360171-63-6 phenyl[4-(4-tert-butylphenyl)-2-(4-methoxyphenyl)phenyl]methanone 
• 1360171-69-2 2-benzoyl-5-(hept-1-ynyl)phenyl trifluoromethanesulfonate 
• 1360171-66-9 [2,4-bis(3-tolylethynyl)phenyl]phenylmethanone 
• 1360171-58-9 4-benzoyl-3'-methoxybiphenyl-3-yl trifluoromethanesulfonate 
• 1360171-46-5 [2,4-bis(p-tolyl)phenyl]phenylmethanone 
• 1360171-50-1 4-benzoyl-4'-methylbiphenyl-3-yl trifluoromethanesulfonate 
• 1360171-48-7 [2,4-bis(3-chlorophenyl)phenyl]phenylmethanone 
• 1360171-56-7 4-benzoyl-3'-chlorobiphenyl-3-yl trifluoromethanesulfonate 
• 1360171-49-8 [2,4-bis(4-methoxyphenyl)phenyl]phenylmethanone 
• 1360171-60-3 4-benzoyl-4'-methoxybiphenyl-3-yl trifluoromethanesulfonate 
• 1360171-52-3 4-benzoyl-3',4'-dimethylbiphenyl-3-yl trifluoromethanesulfonate 
• 1360171-51-2 4-benzoyl-4'-ethylbiphenyl-3-yl trifluoromethanesulfonate 

Relevant articles and documents

Synthesis of functionalized 3,4-diarylbenzophenones and 2,4-diarylbenzophenones by site-selective Suzuki and Sonogashira cross-coupling reactions of bis(triflates) of 3,4- and 2,4-dihydroxybenzophenone

Palladium(0)-catalyzed Suzuki and Sonogashira cross-coupling reactions of the bis(triflates) of 2,4- and 3,4-dihydroxybenzophenone afforded 2,4- and 3,4-diarylbenzophenones, respectively. The reactions proceeded with very good site-selectivity in favor of