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  2. Cinnamaldehyde - Wikipedia

    en.wikipedia.org/wiki/Cinnamaldehyde

    Cinnamaldehyde is used in agriculture because of its low toxicity, but it is a skin irritant. [25] Cinnamaldehyde may cause allergic contact stomatitis in sensitised individuals, however allergy to the compound is believed to be uncommon. [26] Cinnamaldehyde can contain traces of styrene, which arises during storage or transport. Styrene ...

  3. Cinnamic acid - Wikipedia

    en.wikipedia.org/wiki/Cinnamic_acid

    It is obtained from oil of cinnamon, or from balsams such as storax. [4] It is also found in shea butter. [citation needed] Cinnamic acid has a honey-like odor; [2] and its more volatile ethyl ester, ethyl cinnamate, is a flavor component in the essential oil of cinnamon, in which related cinnamaldehyde is the major constituent.

  4. α-Hexylcinnamaldehyde - Wikipedia

    en.wikipedia.org/wiki/Α-Hexylcinnamaldehyde

    The commercial material often contains low levels of 2,6-di-tert-butyl-4-methoxyphenol as a stabilizer. It is a derivative of cinnamaldehyde with a hexyl substituent. One supplier reported that its hexyl cinnamaldehyde (or "hexyl cinnamic aldehyde") contained at least 90% trans isomer. [2]

  5. Ethyl cinnamate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_cinnamate

    Ethyl cinnamate is the ester of cinnamic acid and ethanol.It is present in the essential oil of cinnamon. [citation needed] Pure ethyl cinnamate has a "fruity and balsamic odor, reminiscent of cinnamon with an amber note".

  6. Conjugated system - Wikipedia

    en.wikipedia.org/wiki/Conjugated_system

    Cinnamaldehyde is a naturally-occurring compound that has a conjugated system penta-1,3-diene is a molecule with a conjugated system Diazomethane conjugated pi-system. In theoretical chemistry, a conjugated system is a system of connected p-orbitals with delocalized electrons in a molecule, which in general lowers the overall energy of the molecule and increases stability.

  7. C5H10 - Wikipedia

    en.wikipedia.org/wiki/C5H10

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  8. Sinapaldehyde - Wikipedia

    en.wikipedia.org/wiki/Sinapaldehyde

    It is a derivative of cinnamaldehyde, featuring one hydroxy group and two methoxy groups as substituents. It is an intermediate in the formation of sinapyl alcohol , a lignol that is a major precursor to lignin .

  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. Aldehydes are a common motif in many ...