cyclooctanone, organic, compound, with, formula, waxy, white, solid, identifiers, number, model, jsmol, interactive, image, chembl, chembl18737, chemspider, 9974, echa, infocard, number, pubchem, 10403, unii, z4go9p8suz, comptox, dashboard, dtxsid3060114, inch. Cyclooctanone is an organic compound with the formula CH2 7CO It is a waxy white solid Cyclooctanone Identifiers CAS Number 502 49 8 Y 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 7H2Key IIRFCWANHMSDCG UHFFFAOYSA N SMILES C1CCCC O CCC1 Properties Chemical formula C 8H 14O 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 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 Contents 1 Synthesis 2 Use 3 See also 4 ReferencesSynthesis editIt can be prepared by Jones oxidation of cyclooctanol It can also be produced by ketonization reaction starting with azelaic acid 2 Use editUse of cyclooctanone is almost nonexistent drug chemistry with only 2 known exceptions Blonanserin IprindoleSee also editSuberoneReferences edit Cyclooctanone pubchem ncbi nlm nih gov E J Eisenbraun 1965 Cyclooctanone Organic Syntheses 45 28 doi 10 15227 orgsyn 045 0028 nbsp This organic chemistry article is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Cyclooctanone amp oldid 1181895894, wikipedia, wiki, book, books, library,
