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Cinnamaldehyde is an organic compound with the formula or C₆H₅CH=CHCHO. Occurring naturally as predominantly the trans ( E ) isomer, it gives cinnamon its flavor and odor . [ 1 ] It is a phenylpropanoid that is naturally synthesized by the shikimate pathway . [ 2 ]
Cinnamaldehyde, an organic compound with the formula C 6 H 5 CH=CHCHO; 1-Indanone, the organic compound with the formula C 6 H 4 (CH 2) 2 CO This page was last ...
This is an accepted version of this page This is the latest accepted revision, reviewed on 27 January 2025. Spice from the inner tree bark of several members of genus Cinnamomum This article is about the spice. For the genus of trees where cinnamon originates, see Cinnamomum. For other uses, see Cinnamon (disambiguation). Dried bark strips, bark powder and flowers of the small tree Cinnamomum ...
In enzymology, a cinnamyl-alcohol dehydrogenase (EC 1.1.1.195) is an enzyme that catalyzes the chemical reaction. cinnamyl alcohol + NADP + cinnamaldehyde + NADPH + H +. Thus, the two substrates of this enzyme are cinnamyl alcohol and NADP +, whereas its 3 products are cinnamaldehyde, NADPH, and H +.
Cinnamoyl-CoA reductase (EC 1.2.1.44), systematically named cinnamaldehyde:NADP+ oxidoreductase (CoA-cinnamoylating) but commonly referred to by the acronym CCR, is an enzyme that catalyzes the reduction of a substituted cinnamoyl-CoA to its corresponding cinnamaldehyde, utilizing NADPH and H + and releasing free CoA and NADP + in the process. [1]
It is produced by the hydrogenation of cinnamaldehyde. The compound is used in many mechanistic studies. [1] It is a common substrate in organic synthesis. [2] [3]
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 .
Amygdalin 2 H 2 O HCN benzaldehyde 2 × glucose 2 × Benzaldehyde contributes to the scent of oyster mushrooms (Pleurotus ostreatus). Reactions Benzaldehyde is easily oxidized to benzoic acid in air at room temperature, causing a common impurity in laboratory samples. Since the boiling point of benzoic acid is much higher than that of benzaldehyde, it may be purified by distillation. Benzyl ...