93351-35-0

Upstream product

• 53631-77-9 3-hydroxybenzoic acid 1-methylethyl ester 
• 74-88-4 methyl iodide 
• 99-06-9 3-Carboxyphenol 
• 163396-65-4 3-isopropoxy-4,4-diisopropyl-3-(3-methoxyphenyl)-1,2-dioxetane 

Downstream Products

• 163396-62-1 3-[3-(t-butyldimethylsiloxy)phenyl]-3-isopropoxy-4,4-diisopropyl-1,2-dioxetane 
• 163396-65-4 3-isopropoxy-4,4-diisopropyl-3-(3-methoxyphenyl)-1,2-dioxetane 
• 163396-58-5 2-[3-(t-butyldimethylsiloxy)phenyl]-2-isopropoxy-1,1-diisopropylethene 
• 163396-54-1 2-isopropoxy-1,1-diisopropyl-2-(3-methoxyphenyl)ethene 

Relevant academic research and scientific papers

Regioisomeric preferences in the orthomanganation of meta-substituted acetophenones and isopropyl benzoates, and application of iodo-demanganation with iodine chloride to the synthesis of 2-iodo-3-O-substituted and other ortho-iodo arylcarbonyl compounds

Synthesis is reported of regioisomeric ortho-[Mn(CO)4] derivatives of aryl ketones (2-chlorothioxanthen-9-one and 3′,4′-methylenedioxyacetophenone) and esters (isopropyl 3-methoxy- and 3-acetoxy-benzoate), as well as of the single ortho-[Mn(CO)

Thermal Stability and Chemiluminescence of 3-Alkoxy-3-aryl-4,4-diisopropyl-1,2-dioxetanes

The singlet oxygenation of alkenes 1 gives the corresponding dioxetanes 2, whose thermal stability and half-life of chemiluminescence induced by TBAF (NBun4F) are significantly affected by the 3-alkoxyl group.