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  2. Cyclohexylmethanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylmethanol

    The resulting cyclohexanecarboxaldehyde is then hydrogenated to give the alcohol. [5] [6] References

  3. Magyar Televízió - Wikipedia

    en.wikipedia.org/wiki/Magyar_Televízió

    Magyar Televízió (Hungarian pronunciation: [ˈmɒɟɒr ˈtɛlɛviːzijoː], Hungarian Television) or MTV is a nationwide public television broadcasting organization in Hungary. Headquartered in Budapest , it is the oldest television broadcaster in Hungary and today airs five channels: M1 HD , M2 HD , M3 , M4 Sport and M5.

  4. Hydroxyisohexyl 3-cyclohexene carboxaldehyde - Wikipedia

    en.wikipedia.org/?title=Hydroxyisohexyl_3...

    This page was last edited on 23 February 2012, at 18:26 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  5. M3 (Hungarian TV channel) - Wikipedia

    en.wikipedia.org/wiki/M3_(Hungarian_TV_channel)

    Logo of M3D, before the launch of M3. M3 (M Három) is a Hungarian pay television channel owned and operated by Duna Média since 2015.. The channel launched as M3D, Hungary's first 3D television channel that operated between 25 June and 13 August 2012, the end of the 2012 Summer Olympics.

  6. TV2 (Hungarian TV channel) - Wikipedia

    en.wikipedia.org/wiki/TV2_(Hungarian_TV_channel)

    TV2 (TV Kettő) is a Hungarian free-to-air television channel operating since 4 October 1997, providing a large variety of programming. It is a competitor with RTL for the first place in Hungarian television ratings.

  7. Alkyl cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Alkyl_cycloalkane

    The naming of polycyclic alkanes is more complex, with the base name indicating the number of carbons in the ring system, a prefix indicating the number of rings (e.g., "bicyclo"), and a numeric prefix before that indicating the number of carbons in each part of each ring, exclusive of vertices.

  8. Hydroxymethylpentylcyclohexenecarboxaldehyde - Wikipedia

    en.wikipedia.org/wiki/Hydroxymethylpentylcyclo...

    Typical synthesis starts from myrcene [2] and involves a Diels–Alder reaction with acrolein to produce the cyclohexenecarbaldehyde group, this species is marketed as a fragrance in its own right, most commonly under the name 'myrac aldehyde'.

  9. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    Aldehyde structure. In organic chemistry, an aldehyde (/ ˈ æ l d ɪ h aɪ d /) is an organic compound containing a functional group with the structure R−CH=O. [1] The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl group.