Cyclooctanone

Cyclooctanone
Identifiers
CAS Number
  • 502-49-8 checkY
3D model (JSmol)
  • Interactive image
ChEMBL
  • ChEMBL18737
ChemSpider
  • 9974
ECHA InfoCard 100.007.219 Edit this at Wikidata
EC Number
  • 207-940-2
PubChem CID
  • 10403
UNII
  • Z4GO9P8SUZ
CompTox Dashboard (EPA)
  • DTXSID3060114 Edit this at Wikidata
InChI
  • InChI=1S/C8H14O/c9-8-6-4-2-1-3-5-7-8/h1-7H2
    Key: IIRFCWANHMSDCG-UHFFFAOYSA-N
  • 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 labelling:[1]
Pictograms
 GHS05: CorrosiveGHS07: Exclamation mark
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
Chemical compound

Cyclooctanone is an organic compound with the formula (CH2)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.[2]

Use

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

  1. Blonanserin
  2. Iprindole

See also

References

  1. ^ "Cyclooctanone". pubchem.ncbi.nlm.nih.gov.
  2. ^ E. J. Eisenbraun (1965). "Cycloöctanone". Organic Syntheses. 45: 28. doi:10.15227/orgsyn.045.0028.
  • v
  • t
  • e