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Pentanones
Pentanone may refer to the following ketones containing five carbon atoms: * 2-Pentanone (Methyl propyl ketone, MPK) ** 3-Methyl-2-butanone (Methyl isopropyl ketone, MIPK) * 3-Pentanone (Diethyl ketone, DEK) See also * Cyclopentanone Cyclopentanone is the organic compound with the formula (CH2)4CO. This cyclic ketone is a colorless volatile liquid. Preparation Ketonic decarboxylation of adipic acid gives cyclopentanone. The reaction is conducted at elevated temperatures in t ... {{Chemistry index ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
3-Methyl-2-butanone
3-Methyl-2-butanone (methyl isopropyl ketone, MIPK) is a ketone and solvent of minor importance. It is comparable to MEK (Methyl ethyl ketone), but has a lower solvency and is more expensive.{{citation , author=Dieter Stoye , contribution=Solvents , title=Ullmann's Encyclopedia of Industrial Chemistry ''Ullmann's Encyclopedia of Industrial Chemistry'' is a major reference work related to Chemical industry, industrial chemistry by chemist Fritz Ullmann, first published in 1914, and exclusively in German as "Enzyklopädie der Technischen Chemie ... , edition=7th , publisher=Wiley , year=2007 , pages=55–56 References Pentanones Ketone solvents ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Ketone
In organic chemistry, a ketone is an organic compound with the structure , where R and R' can be a variety of carbon-containing substituents. Ketones contain a carbonyl group (a carbon-oxygen double bond C=O). The simplest ketone is acetone (where R and R' are methyl), with the formula . Many ketones are of great importance in biology and industry. Examples include many sugars (ketoses), many steroids, ''e.g.'', testosterone, and the solvent acetone. Nomenclature and etymology The word ''ketone'' is derived from ''Aketon'', an old German word for ''acetone''. According to the rules of IUPAC nomenclature, ketone names are derived by changing the suffix ''-ane'' of the parent alkane to ''-anone''. Typically, the position of the carbonyl group is denoted by a number, but traditional nonsystematic names are still generally used for the most important ketones, for example acetone and benzophenone. These nonsystematic names are considered retained IUPAC names, although some introdu ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cyclopentanone
Cyclopentanone is the organic compound with the formula (CH2)4CO. This cyclic ketone is a colorless volatile liquid. Preparation Ketonic decarboxylation of adipic acid gives cyclopentanone. The reaction is conducted at elevated temperatures in the presence of barium hydroxide. : The Pd-catalyzed oxidation of cyclopentene also gives cyclopentanone. Uses Cyclopentanone is common precursor to fragrances, especially those related to jasmine and jasmone. Examples include 2-pentyl- and 2-heptylcyclopentanone. It is a versatile synthetic intermediate, being a precursor to cyclopentobarbital. Cyclopentanone is also used to make cyclopentamine, the pesticide pencycuron, and pentethylcyclanone. It is also used as a precursor to cubane-1,4-dicarboxylate, which is used to synthesize other substituted cubanes, such as the high explosives heptanitrocubane and octanitrocubane. References {{Authority control Cycloalkanones, 5 Ketone solvents Perfume ingredients Cyclopentanes ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
