14860-89-0

Usage

InChI:InChI=1/C12H18O/c1-9(2)10-6-5-7-11(8-10)12(3,4)13/h5-9,13H,1-4H3

Upstream product

• 80-24-0 3-isopropyl-1-(2-hydroperoxy-2-propyl)benzene 
• 99-62-7 1,3-diisopropylbenzene 
• 80937-33-3 oxygen 
• 13387-60-5 3-(2-hydroxy-2-propyl)-1-(2-hydroperoxy-2-propyl)benzene 

Downstream Products

• 13387-60-5 3-(2-hydroxy-2-propyl)-1-(2-hydroperoxy-2-propyl)benzene 
• 19936-08-4 1-(α-chloro-isopropyl)-3-isopropyl-benzene 

Relevant academic research and scientific papers

Process for the production of a dihydroxybenzene and dicarbinol from diisopropylbenzene

Improved methods for the simultaneous production of dihydroxybenzene and dicarbinol from diisopropylbenzene are provided. These methods provide for continuous and simultaneous production of diisopropylbenzene dihydroperoxide (DHP) and diisopropylbenzene hydroxyhydroperoxide (HHP) using Karr Column extractors operated in series. A very high purity DHP-containing solution, the precursor to the dihydroxybenzene, can be produced according to the reported methods. A safe and efficient method for producing dicarbinol from HHP is also disclosed.

The substrate specificity of cytochrome P450(cam)

The catalytic turnover of xenobiotics by cytochrome P450(cam) results in both the formation of organic metabolites and the uncoupled production of H2O2, and H2O. Previous studies have shown that a receptor-constrained thre