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The page provides a comprehensive list of isomers of dodecane, including their chemical structures and properties.
3-Ethylpentane (C 7 H 16) is a branched saturated hydrocarbon. It is an alkane, and one of the many structural isomers of heptane, consisting of a five carbon chain with a two carbon branch at the middle carbon. An example of an alcohol derived from 3-ethylpentane is the tertiary alcohol 3-ethylpentan-3-ol. [3]
3-Hexanone (ethyl propyl ketone) is an organic compound with the formula C 6 H 12 O. It is a ketone used as a solvent and as a chemical intermediate. According to IFF, it was described as having Sweet, Fruity, Waxy, Grape organoleptic properties.
3-Pentanone (also known as diethyl ketone) is a simple, symmetrical dialkyl ketone. It is a colorless liquid ketone with an odor like that of acetone . It is soluble in about 25 parts water, but miscible with organic solvents.
3-Octanone is an organic compound with the formula C 5 H 11 C(O)C 2 H 5. A colorless fragrant liquid, it is classified as a ketone . It is one of three octanones, the others being 2-octanone and 4-octanone.
Ethyl group (highlighted blue) as part of a molecule, as the ethyl radical, and in the compounds ethanol, bromoethane, ethyl acetate, and ethyl methyl ether. In organic chemistry , an ethyl group (abbr. Et ) is an alkyl substituent with the formula −CH 2 CH 3 , derived from ethane ( C 2 H 6 ).
Pentyl is a five-carbon alkyl group or substituent with chemical formula-C 5 H 11. It is the substituent form of the alkane pentane . In older literature, the common non-systematic name amyl was often used for the pentyl group.
3-Ethyl-3-pentanol, also known as 3-ethylpentan-3-ol, is a tertiary alcohol with the molecular formula C 7 H 16 O. It reacts with chromic acid by first dehydrating to an olefin 3-ethyl-2-pentene, and then by converting the double bond to an epoxide. [2] Perfluorination affords perfluorotriethylcarbinol, a powerful uncoupling agent.