Methyl acetophenone amyl-ketone

Aldehydes and ketones. n-Butyraldehyde Acetone Methyl n-amyl ketone Benzaldehyde Acetophenone Benzophenone. 

Butylacetone. See Methyl n-amyl ketone 4-t-Butylacetophenone 4 -t-Butylacetophenone. See p-t-Butyl acetophenone p-t-Butyl acetophenone CAS 943-27-1 EINECS/ELINCS 213-399-3 Synonyms Acetophenone, 4 -t-butyl- 4-t-Butylacetophenone 4 -t-Butylacetophenone Ethanone, 1-[4-(1,1-dimethylethyl) phenyl]-Empirical C12H16O Properties M.w. 176.26 Uses Fragrance in cosmetics Manuf./Distrib. ABCR http //www.abcr.de, Acros Org. http //www.acros.be] Advanced Synthesis Tech, http //www.advancedsynthesis.com] Alfa Aesar http //www.aifa.com] Fluorochem USA http //WWW. fiuorochemusa. com Butyl acetoxystearate Empirical C24H46O4... 

Methoxy-4-vinylphenol Methyl acetate 4 -Methyl acetophenone 2-Methylallyl butyrate Methyl n-amyl ketone... 

Methoxy-4-vinylphenol Methyl abietate 4 -Methyl acetophenone Methyl acetylaminobenzoate Methyl amyl alcohol Methyl n-amyl ketone Methyl o-anisate Methyl p-anisate Methyl anthranilate 2-Methyl benzoxazole... 

On the other hand, Gavrilova and Gonikberg opened the furan ring with hydrogen, without the use of catalysts.213 The reaction is carried out at high temperature (350-375°) and at a pressure between 240 and 750 atmospheres, in the absence of a solvent. The following products are obtained from 2-methylfuran acetone, methyl ethyl ketone, methyl butyl ketone, methyl amyl ketone, acetophenone, methylpropylcarbinol, w-pentane, and water. The authors suggest that these products are formed by a free radical mechanism. 

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