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  • methanol
  • CHM with a methylethyl (or isopropyl) substituent group at the same position as the methyl group in 4-methylcyclohexanemethanol (cis-4-(1-methylethyl) cyclohexane methanol, CAS 13828-37-0) is regarded as a flavoring and fragrance agent, sometimes listed under the synonym p-menthan-7-ol, and was the subject of a review article on its toxicological and dermatological properties in 2008. (wikipedia.org)
  • alkane
  • The six-membered ring of the alkane, cyclohexane, has the 'chair' as its preferred conformation and through proton NMR it would be expected that the produced spectrum would show the different sorts of protons (axial and equatorial) resonating at different frequencies, and so two signals would be seen, due to the protons being in slightly different chemical environments. (wikipedia.org)
  • Diffusion
  • This chapter provides the diffusion coefficient of benzene in cyclohexane at different concentrations measured using Taylor dispersion technique, Rayleigh interferometry, open ended capillary, NMR spin echo pulse gradient, NMR spin echo field gradient, Gouy interferometry, forced Rayleigh scattering, diaphragm cell and closed capillary. (springer.com)
  • Winkelmann J. (2018) Diffusion coefficient of benzene in cyclohexane. (springer.com)
  • This chapter provides the diffusion coefficient of methyl-cyclohexane in heptan-1-ol at different concentrations measured using diaphragm cell. (springer.com)
  • Winkelmann J. (2018) Diffusion coefficient of methyl-cyclohexane in heptan-1-ol. (springer.com)
  • atoms
  • In the case of the catalytic hydrogenation the aromatic part of the diisononyl phthalate is transformed to a cyclohexane ring by a formal addition of 6 hydrogen atoms while the alkyl and ester groups are not affected by the hydrogenation. (wikipedia.org)
  • chemical
  • This page provides supplementary chemical data on cyclohexane. (wikipedia.org)
  • Cyclohexane-1,2-diol is a chemical compound found in castoreum. (wikipedia.org)
  • However, the chemical reactivity of cyclohexane, is inconsistent with two types of hydrogens in a stable form of the molecule (for example, there is only one monochlorocyclohexane, not two, as would be predicted if axial and equatorial hydrogens could be replaced independently), but this is due to the presence of rapid ring inversion as explained above. (wikipedia.org)
  • chair
  • In 1890, Hermann Sachse, a 28-year-old assistant in Berlin, published instructions for folding a piece of paper to represent two forms of cyclohexane he called symmetrical and unsymmetrical (what we would now call chair and boat). (wikipedia.org)