Cyclooctanone

Cyclooctanone
Identifiers
CAS Number	502-49-8 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL18737;
ChemSpider	9974;
ECHA InfoCard	100.007.219
EC Number	207-940-2;
PubChem CID	10403;
UNII	Z4GO9P8SUZ;
CompTox Dashboard (EPA)	DTXSID3060114 ;
	InChI InChI=1S/C8H14O/c9-8-6-4-2-1-3-5-7-8/h1-7H2 Key: IIRFCWANHMSDCG-UHFFFAOYSA-N;
	SMILES C1CCCC(=O)CCC1;
Properties
Chemical formula	C8H14O
Molar mass	126.199 g·mol−1
Appearance	colorless solid
Density	0.956 g/cm3
Melting point	29 °C (84 °F; 302 K)
Boiling point	86 12 torr
Refractive index (nD)	0.959
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H315, H319, H335
Precautionary statements	P260, P261, P264, P264+P265, P271, P280, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P351+P338, P305+P354+P338, P316, P319, P321, P332+P317, P337+P317, P362+P364, P363, P403+P233, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Cyclooctanone is an organic compound with the formula (CH₂)₇CO. It is a waxy white solid.

Synthesis and reactions

It can be prepared by

Among its many reactions, Baeyer-Villiger oxidation gives the nine-membered cyclic ester.^[4]

^ "Cyclooctanone". pubchem.ncbi.nlm.nih.gov.
^ Dess, Daniel B.; Martin, J. C. (1991). "A useful 12-I-5 triacetoxyperiodinane (The Dess-Martin periodinane) for the selective oxidation of primary or secondary alcohols and a variety of related 12-I-5 species". Journal of the American Chemical Society. 113 (19): 7277–7287. doi:10.1021/ja00019a027.
^ E. J. Eisenbraun (1965). "Cycloöctanone". Organic Syntheses. 45: 28. doi:10.15227/orgsyn.045.0028.
^ Krow, Grant R. (1993). "TheBaeyer–VilligerOxidation of Ketones and Aldehydes". Organic Reactions. pp. 251–798. doi:10.1002/0471264180.or043.03. ISBN 978-0-471-26418-7.

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