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<p>Its color is due to the ? -> ?* transition: increased conjugation in comparison with acrolein shifts this band towards the visible.</p>

<p>The molecule can be identified by characteristic spectroscopic signals. Infrared spectra show strong absorption bands near 1685 cm<sup>-1</sup> (C=O stretch) and 1620 cm<sup>-1</sup> (C=C stretch). In the proton nuclear magnetic resonance (<sup>1</sup>H NMR) spectrum, the aldehydic proton resonates around 9.6 ppm, while aromatic and vinyl protons appear between 6.3 and 7.6 ppm.</p>

<p><big>Biosynthesis</big></p>
<p>Cinnamaldehyde</p><p>
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