Chemistry:Cyclooctanone

Cyclooctanone

Identifiers
CAS Number	502-49-8 Y
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL18737
ChemSpider	9974
EC Number	207-940-2
PubChem CID	10403
UNII	Z4GO9P8SUZ
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
Melting point	42 °C (108 °F; 315 K)
Refractive index (nD)	0.959
Hazards
GHS pictograms
GHS Signal word	Danger
GHS hazard statements	H315, H319, H335
GHS precautionary statements	P260, P261, P264, P264+265Category:GHS errors, P271, P280, P301+330+331, P302+352, P302+361+354Category:GHS errors, P304+340, P305+351+338, P305+354+338Category:GHS errors, P316Category:GHS errors, P319Category:GHS errors, P321, P332+317Category:GHS errors, P337+317Category:GHS errors, P362+364Category:GHS errors, P363, P403+233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Tracking categories (test):

• SizeSet

Cyclooctanone is an organic compound with the formula (CH
2)
7CO. It is a waxy white solid.

Synthesis

• It can be prepared by Jones oxidation of cyclooctanol.
• It can also be produced by ketonization reaction starting with azelaic acid.

Use

Use of cyclooctanone is almost nonexistent drug chemistry with only 2 known exceptions:

1. Blonanserin
2. Iprindole

See also

• Suberone