39615-37-7

Upstream product

• 2142-69-0 2-bromophenyl methyl ketone 
• 7073-70-3 1-bromo-2-isopropenylbenzene 
• 630-19-3 pivalaldehyde 

Downstream Products

• 892121-21-0 1-tert-butyl-4-(4-tert-butyl-phenylsulfanylmethyl)-1-methoxy-4-methyl-1,4-dihydro-benzo[d][1,2]dioxine 
• 892121-23-2 1-tert-butyl-4-(4-tert-butyl-phenylsulfanylmethyl)-4-methyl-1,4-dihydro-benzo[d][1,2]dioxin-1-ol 
• 676593-28-5 1-(2-isopropenylphenyl)-2,2-dimethylpropan-1-one 
• 39615-39-9 1-(2-isopropylphenyl)-2,2-dimethylpropan-1-ol 

Relevant academic research and scientific papers

Convenient synthesis of 1,3-dihydroisobenzofurans by hydriodic acid-catalyzed cyclization of 2-vinylbenzyl alcohols

A new and short process has been developed for the preparation of 1,1,3-tri- and 1,1,3,3-tetra-sub stituted 1,3-dihydroisobenzofurans (phthalanes) from α-substituted 2-bromostyrenes. The method involves addition of α-substituted 2-lithiostyrenes, generate

Ground state oxygen in synthesis of cyclic peroxides. Part 1: Benzo fused ketals

A thiol-olefin-cooxygenation (TOCO) radical chain reaction involving ground state molecular oxygen converts 2′-isopropenyl acetophenones directly into cyclic peroxy hemiketal products with three new bonds. Starting with 4-t-butylbenzenethiol, this TOCO pr