23454-06-0

Upstream product

• 404-19-3 2-chloro-1,2-difluoro-1-(phenyl thio) ethylene 
• 91122-75-7 2-chloro-1,1,2-trifluoro-1-(phenyl thio) ethane 
• 108-98-5 thiophenol 
• 23451-85-6 <1,2,2-Trichlor-1,2-difluor-aethyl>-phenyl-sulfid 
• 23451-83-4 <1,2-Dibrom-2-chlor-1,2-difluor-aethyl>-phenyl-sulfid 

Downstream Products

• 23453-83-0 Fluor-phenylsulfonyl-essigsaeure-diethylamid 
• 23454-09-3 1,2-Difluor-1-phenylsulfenyl-2-<4-chlor-phenylsulfonyl>-aethylen 
• 23531-40-0 N,N'-Di-p-tolyl-fluor-phenylsulfonyl-essigsaeure-amidin 
• 23454-04-8 <1,2,2,2-Tetrafluor-aethyl>-phenyl-sulfon 

Relevant academic research and scientific papers

Microwave activated Diels-Alder Cycloaddition reactions of 1,2-difluoro- 1-chlorovinylphenylsulfone

Diels-Alder Cycloadditions of 1,2-difluoro-1-chlorovinylphenylsulfone with cyclopentadiene, furan and 1,3-diphenylisobenzofuran are studied under thermal and microwave activation conditions. Microwave heating is found to be more efficient method for condensation of fluorinated dienophile with dienes.