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The main use of ozonolysis is for the conversion of unsaturated fatty acids to value-added derivatives. Ozonolysis of oleic acid is an important route to azelaic acid. The coproduct is nonanoic acid: [20] CH 3 (CH 2) 7 CH=CH(CH 2) 7 CO 2 H} + 4 O 3 → HO 2 C(CH 2) 7 CO 2 H} + CH 3 (CH 2) 7 CO 2 H
Methylpentene is an alkene with a molecular formula C 6 H 12.The prefix "methyl-" is derived from the fact that there is a methyl(CH 3) branch, the word root "-pent-" is derived from the fact that there are 5 carbon atoms in the parent chain, while the "-ene" suffix denotes that there is a double bond present, as per IUPAC nomenclature. [1]
R)-2-Methylpent-4-enoic acid can also be used in synthesis of other chiral compounds. For example, it has been used in the process of synthesizing the drug Sacubitril as a reagent for adding a chiral center to the molecule.
Pentenes are alkenes with the chemical formula C 5 H 10.Each molecule contains one double bond within its molecular structure. Six different compounds are in this class, differing from each other by whether the carbon atoms are attached linearly or in a branched structure and whether the double bond has a cis or trans form.
Download as PDF; Printable version; ... trans-2-pentene (CAS 646-04-8) Butenes. 2-Methyl-1-butene (CAS 563-46-2) ... Toggle the table of contents. C 5 H 10.
Download as PDF; Printable version; ... 2-Pentyne, an organic compound ... Toggle the table of contents. 2-Pentyne. 16 languages ...
Perfluoro(2-methyl-3-pentanone) is a fluorinated ketone with the structural formula CF 3 CF 2 C(=O)CF(CF 3) 2, a fully-fluorinated analog of ethyl isopropyl ketone. It is used as an electronics coolant liquid and fire protection fluid sold commercially by 3M under brand names such as Novec 1230, Novec 649, and FK-5-1-12. It is also known as ...
In the example below, the disrotation causes both methyls to point upwards, causing the product to be cis-dimethylcyclohexadiene. In addition, the torquoselectivity in an electrocyclic reaction refers to the direction of rotation. For example, a reaction that is conrotatory can still rotate in two directions, producing enantiomeric products.