acetophenone การใช้

• The drug is the ketal formed between algestone and acetophenone.
• The result indicated that the products contain styrene, acetophenone and brominated substances.
• Acetophenone is then reduced to an alcohol and conjugated by glutathione transferases .,
• In contrast to acetophenone which contains only 8 hydrogens, cyclopentadecanone has 28.
• For instance, acetophenone, ethyl acetate and acetone
• Products of decomposition of cumene hydroperoxide are methylstyrene, acetophenone, and cumyl alcohol.
• In these experiments, acetophenone's odor was shown to activates an odorant receptor ( Olfr151 ) in mice.
• In the second reaction sequence, [ Carbonyl-14C ]-2-hydroxy-acetophenone was used first.
• This has been shown in experiments that use Acetophenone to examine the inheritance of parental traumatic exposure ( odor fear conditioning ).
• The study reports that drosophila melanogaster ( fruit fly ), which is ordinarily attracted to acetophenone, spontaneously dislikes deuterated acetophenone.
• The study reports that drosophila melanogaster ( fruit fly ), which is ordinarily attracted to acetophenone, spontaneously dislikes deuterated acetophenone.
• In one example, Clark et al . estimate 0.9 kg of AlCl 3 is wasted per kilogram of dimethyl acetophenone produced.
• Compound XII was formed from condensation of [ carbonyl-14C-]-2-hydroxy-acetophenone with dimethyl oxylate and ring closure.
• An example with modified reagents ( sulfur, concentrated ammonium hydroxide and pyridine ) is the conversion of acetophenone to 2-phenylacetamide and phenylacetic acid:
• "' Acetosyringone "'is a phenolic natural product, and is a chemical compound related to acetophenone and 2, 6-dimethoxyphenol.
• Malic acid can be used for apple flavor, allyl hexanoate for pineapple, ethyl propionate for fruit punch, cinnamic aldehyde for cinnamon and acetophenone for cherry.
• In 2013, Turin and coworkers confirmed Vosshall and Keller's experiments showing that even trained human subjects were unable to distinguish acetophenone from its deuterated counterpart.
• However, the reaction was pioneered a year earlier in 1893 by Konovalov, who converted the potassium salt of 1-phenylnitroethane with sulfuric acid to acetophenone.
• A 2013 study published in " Nature Neuroscience " reported that mice trained to fear the smell of a chemical called acetophenone passed their fear onto at least two generations.
• To account for the different results seen with acetophenone and cyclopentadecanone, Turin and coworkers assert that " there must be many C-H bonds before they are detectable by smell.