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・ Phenylglyoxylate dehydrogenase (acylating)
・ Phenylglyoxylic acid
・ Phenylhydrazine
・ Phenylhydroxylamine
・ Phenylisobutylamine
・ Phenylisocyanate
・ Phenylketonuria
・ Phenyllithium
・ Phenylmagnesium bromide
・ Phenylmercuric borate
・ Phenylmercury acetate
・ Phenylobacterium immobile
・ Phenylphosphine
・ Phenylpiperazine
・ Phenylpiperidine
Phenylpropanoic acid
・ Phenylpropanoid
・ Phenylpropanoids metabolism
・ Phenylpropanolamine
・ Phenylpropene
・ Phenylpropiolic acid
・ Phenylpropylaminopentane
・ Phenylpyruvate decarboxylase
・ Phenylpyruvate tautomerase
・ Phenylpyruvic acid
・ Phenylserine aldolase
・ Phenylsilane
・ Phenylsilatrane
・ Phenylsulfinic acid
・ Phenylthiocarbamide


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Phenylpropanoic acid : ウィキペディア英語版
Phenylpropanoic acid

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Phenylpropanoic acid or hydrocinnamic acid is a carboxylic acid with the formula C9H10O2 belonging to the class of phenylpropanoids. It is a white, crystalline solid with a sweet, floral scent at room temperature. Phenylpropanoic acid has a wide variety of uses including cosmetics, food additives, and pharmaceuticals.〔S. M. Korneev "Hydrocinnamic Acids: Application and Strategy of Synthesis" Synthesis 2013, volume 45(8), pages 1000-1015. 〕
== Preparation and reactions==
Phenylpropanoic acid can be prepared from cinnamic acid by hydrogenation.〔 Originally it was prepared by reduction with sodium amalgam in water and by electrolysis.
A characteristic reaction of phenylpropanoic acid is its cyclization to indanones. When the side chain is homologated by the Arndt–Eistert reaction, subsequent cyclization affords 2-tetralone, derivatives.〔

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