Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

// request.cf · coarse context

A page that knows where it met you.

Only coarse request metadata is shown. This demo does not display or persist visitor IP addresses.

Country
US
Cloudflare location
CMH
Connection
HTTP/2
Language
Not provided

Ray ID: a21ea5208e0bb86e

Jump to content

Methylcyclohexanone

From Wikipedia, the free encyclopedia

Methylcyclohexanones are a group of three isomers: 2-methylcyclohexanone, 3-methylcyclohexanone, and 4-methylcyclohexanone.[1] They can be viewed as derivative of cyclohexanone. They can be prepared by oxidation of methylcyclohexane as well as partial hydrogenation of the corresponding cresols. All are colorless liquids. The 2- and 3-isomers are chiral.

Methylcyclohexanones
IsomerStructureCAS RNm.p. (°C)b.p. (°C)density (g/cm3)
2-Methylcyclohexanone583-60-8−13.9165.10.925
3-Methylcyclohexanone591-24-2−73.5170.00.920
4-Methylcyclohexanone589-92-4−40.6171.30.916

References

[edit]
  1. Musser, Michael Tuttle (2000). "Cyclohexanol and Cyclohexanone". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a08_217. ISBN 3527306730.