Cyclohexylacetone
Names | |
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IUPAC name
1-cyclohexylpropan-2-one | |
Identifiers | |
•622-45-7 | |
3D model (Jmol) | Interactive image |
ChemSpider | 60261 |
ECHA InfoCard | 100.002.858 |
UNII | UL0RS4H1UE |
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Properties | |
C9H16O | |
Molar mass | 140.22 g/mol |
Density | 0.905 |
Boiling point | 198 to 200 °C (388 to 392 °F; 471 to 473 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Cyclohexylacetone (acetonylcyclohexane) is an organic compound. Cyclohexylacetone is closely related to phenylacetone being phenylacetone with the benzene ring replaced with a cyclohexane ring. Similarly to phenylacetone's synthesis, cyclohexylacetone can be prepared by a variant of the Friedel-Crafts reaction (the Darzens–Nenitzescu Synthesis of Ketones) by reacting cyclohexane with chloroacetone.
Applications
Cyclohexylacetone along with N-Methylformamide can be used to make racemic propylhexedrine in a similar fashion to the phenylacetone synthesis of methamphetamine.[1]
Another cyclohexylacetone use is in the production of droprenilamine.
See also
External links
References
- ↑ Merck Index 7761 - Kleeman & Engel p.774 OCDS Vol.1 p.37 (1977) I.N. p.817
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