Rujukan Siklohexanon

  1. ↑ "ICSC 0425 – CYCLOHEXANONE". inchem.org. Retrieved 2022-08-24.
  2. ↑ "CDC – NIOSH Pocket Guide to Chemical Hazards – Cyclohexanone".
  3. 1 2 "Cyclohexanone (CID 7967)". PubChem.
  4. 1 2 3
  5. 1 2
  6. ↑
  7. ↑ "Cyclohexanone (CID 7967)". PubChem.
  8. 1 2 3 4 5 Musser, Michael T. (October 15, 2011). "Cyclohexanol and Cyclohexanone". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KgaA. doi:10.1002/14356007.a08_217.pub2. ISBN 9783527306732. OCLC 46878292. Dicapai pada January 27, 2009.
  9. ↑ Plotkin, Jeffrey S. (2016-03-21). "What's New in Phenol Production?". American Chemical Society. Diarkibkan daripada yang asal pada 2019-10-27. Dicapai pada 2019-10-27.
  10. ↑ "Phenol – The essential chemical industry online". 2017-01-11. Dicapai pada 2019-10-27.
  11. ↑ "Oxidation of Cyclohexanol to Cyclohexanone". Diarkibkan daripada yang asal pada 2012-04-26. Dicapai pada 2012-07-09.
  12. ↑ M. S. Newman, M. D. Farbman, H. Hipsher (1945). "2-chlorocyclohexanone". Org. Synth. 25: 22. doi:10.15227/orgsyn.025.0022.CS1 maint: multiple names: authors list (link)
  13. ↑ Valsamma Varghese, Manasi Saha, Kenneth M. Nicholas (1989). "Alkylations Using Hexacarbonyl(Propargylium)dicobalt Salts: 2-(1-methyl-2-propynyl)cyclohexanone". Org. Synth. 67: 141. doi:10.15227/orgsyn.067.0141.CS1 maint: multiple names: authors list (link)
  14. ↑ R. B. Woodward, I. J. Pachter, M. L. Scheinbaum (1974). "2,2-(Trimethylenedithio)cyclohexanone". Org. Synth. 54: 39. doi:10.15227/orgsyn.054.0039.CS1 maint: multiple names: authors list (link)
  15. ↑ Shulgin, A. T.; MacLean, D. E. (25 September 2008). "Illicit Synthesis of Phencyclidine (PCP) and Several of Its Analogs". Clinical Toxicology. 9 (4): 553–560. doi:10.3109/15563657608988157. PMID 975751.