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Isopropenyl acetate is an organic compound, which is the acetate ester of the enol tautomer of acetone. This colorless liquid is significant commercially as the principal precursor to acetylacetone .
Isopropyl acetate is a solvent with a wide variety of manufacturing uses that is miscible with most other organic solvents, and slightly soluble in water (although less so than ethyl acetate). It is used as a solvent for cellulose, plastics, oil and fats. It is a component of some printing inks [4] and perfumes.
Acetylacetone is prepared industrially by the thermal rearrangement of isopropenyl acetate. [10] Laboratory routes to acetylacetone also begin with acetone. Acetone and acetic anhydride ((CH 3 C(O)) 2 O) upon the addition of boron trifluoride (BF 3) catalyst: [11] (CH 3 C(O)) 2 O + CH 3 C(O)CH 3 → CH 3 C(O)CH 2 C(O)CH 3
In organic chemistry, 1-propenyl (or simply propenyl) has the formula CH=CHCH 3 and 2-propenyl (isopropenyl) ... Isopropenyl acetate is a 2-propenyl ester, ...
Isopropenyl acetate This page was last edited on 12 December 2022, at 05:27 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...
Isopropyl alcohol (IUPAC name propan-2-ol and also called isopropanol or 2-propanol) is a colorless, flammable, organic compound with a pungent alcoholic odor. [9]Isopropyl alcohol, an organic polar molecule, is miscible in water, ethanol, and chloroform, demonstrating its ability to dissolve a wide range of substances including ethyl cellulose, polyvinyl butyral, oils, alkaloids, and natural ...
In a novel kilogram-scale metal-free Meerwein arylation the diazonium salt is formed from 2-nitroaniline, the alkene isopropenyl acetate is an adduct of propyne and acetic acid and the reaction product 2-nitrophenylacetone: [7] Metal free meerwein arylation
From left to right: the two isomeric groups propyl and 1-methylethyl (iPr or isopropyl), and the non-isomeric cyclopropyl group. In organic chemistry, a propyl group is a three-carbon alkyl substituent with chemical formula −CH 2 CH 2 CH 3 for the linear form.