One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Safety of 5-(Bromomethyl)-2,3-dihydro-1,4-benzodioxine, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 214894-89-0, Name is 5-(Bromomethyl)-2,3-dihydro-1,4-benzodioxine, molecular formula is C9H9BrO2
FUNGAL HYDROXYLATION OF ETHYL BENZENE AND DERIVATIVES
The fungus Mortierella isabellina converts ethyl benzene and a number of para-substituted derivatives to the corresponding optically active 1-phenylethanols with enantiomeric excesses between 5 and 40percent.Hydrogen removal from the substrate preceeds product formation and is stereochemically independent of it.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Safety of 5-(Bromomethyl)-2,3-dihydro-1,4-benzodioxine, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 214894-89-0, in my other articles.
Reference£º
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem