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2-Phenylhexane is an aromatic hydrocarbon. It can be produced by a Friedel-Crafts alkylation between 1-chlorohexane and benzene ., [ 1 ] or by the reaction of benzene and 1-hexene with various acid catalysts such as antimony pentafluoride , [ 2 ] scandium(III) triflate , [ 3 ] and phosphoric acid .
3-Ethyl-2-methyldecane; 3-Ethyl-3-methyldecane; 3-Ethyl-4-methyldecane; 3-Ethyl-5-methyldecane; 3-Ethyl-6-methyldecane; 3-Ethyl-7-methyldecane; 3-Ethyl-8-methyldecane
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]
The page provides a comprehensive list of isomers of dodecane, including their chemical structures and properties.
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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.
2-Ethylhexanal is the organic compound with the formula CH 3 CH 2 CH 2 CH 2 CH(C 2 H 5)CHO. A colorless liquid, it is produced on a large scale industrially as a precursor to 2-ethylhexanoic acid and 2-ethylhexanol, both used as precursors to plasticizers. It was studied in the detergent industry since the 1930s. [2]
1189-87-3 C 5 H 12 FO 2 P: propyl ethylphosphonofluoridate: 2992-95-2 C 5 H 12 NO 3 PS 2: dimethoate: 60-51-5 C 5 H 12 NO 4 PS: omethoate: 1113-02-6 C 5 H 12 N 2: butylmethyldiazene: 4426-46-4 C 5 H 12 N 2: homopiperazine: 505-66-8 C 5 H 12 N 2 O: valeric acid hydrazide: 38291-82-6 C 5 H 12 N 3 OP: tetramethylphosphorodiamidic cyanide: 14445-60 ...