1,4-Cyclohexanedione[1] | |
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1,4-Cyclohexanedione |
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Identifiers | |
CAS number | 637-88-7 |
ChemSpider | 11995 |
EC number | 211-306-0 |
KEGG | C08063 |
ChEBI | CHEBI:28286 |
Jmol-3D images | Image 1 |
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Properties | |
Molecular formula | C6H8O2 |
Molar mass | 112.127 g/mol |
Melting point |
77–78.5 °C |
Boiling point |
112 °C |
Hazards | |
S-phrases | S22,S23,S24,S25 |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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Infobox references |
1,4-Cyclohexanedione is the organic compound. This tan or yellow crystalline 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 is prepared in two steps from diesters of succinic acid. For example under basic conditions, the diethyl ester condenses to give 2,5-dicarbethoxy-1,4-cyclohexanedione. This intermediate can be hydrolysed and decarboxylated to afford the desired dione.[2]