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1,4-Cyclohexanedione is an organic compound with the formula (CH 2) 4 (CO) 2. This white solid is one of the three isomeric cyclohexanediones . This particular diketone is used as a building block in the synthesis of more complex molecules.
1,4-Cyclohexanedione This page was last edited on 23 June 2017, at 01:22 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...
1,4-Cyclohexadiene is an organic compound with the formula C 6 H 8. It is a colourless, flammable liquid that is of academic interest as a prototype of a large class of related compounds called terpenoids , an example being γ- terpinene .
Names Preferred IUPAC name. 5,5-Dimethylcyclohexane-1,3-dione. Other names ... Classified as a cyclic diketone, it is a derivative of 1,3-cyclohexanedione.
1,3-Cyclohexanedione Names Preferred IUPAC name. Cyclohexane-1,3-dione. Other names ... 1,3-Cyclohexanedione is an organic compound with the formula (CH 2) 4 (CO) 2.
Cyclohexa-1,3-diene itself is rare in nature, but the cyclohexa-1,3-diene motif is fairly common. [8] One example is chorismic acid, an intermediate in the shikimic acid pathway. Of the several examples of the terpenoids and terpenes, a prominent example is phellandrene. An unusual derivative is cis-1,2-dihydrocatechol.
With strong bases, the positions 4 and 6 (the two CH 2-groups of the carbonyl group and the C-C double bond adjacent) are deprotonated. Cyclohexenone is an in-vitro catalyst for a relatively mild decarboxylation of alpha amino acids .
General structure of 1,2-, 1,3-, and 1,4-dicarbonyls. In organic chemistry, a dicarbonyl is a molecule containing two carbonyl (C=O) groups.Although this term could refer to any organic compound containing two carbonyl groups, it is used more specifically to describe molecules in which both carbonyls are in close enough proximity that their reactivity is changed, such as 1,2-, 1,3-, and 1,4 ...