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  • == Cinnamic Acid == <!--File:Cinnamic acid structure.svg-->[[Chemical structure of cinnamic acid]]
    3 KB (386 words) - 18:27, 21 January 2024

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  • == Cinnamic Acid == <!--File:Cinnamic acid structure.svg-->[[Chemical structure of cinnamic acid]]
    3 KB (386 words) - 18:27, 21 January 2024
  • {{PAGENAME}} - A type of organic compound that is a derivative of cinnamic acid and is found in many plants, including cinnamon.
    180 bytes (25 words) - 23:14, 7 April 2024
  • ...romination]] of trans-cinnamic acid. In this reaction, the trans isomer of cinnamic acid reacts with bromine to form a dibromide product. The stereochemistry o [[File:Bromination of trans-cinnamic acid.png|thumb|Bromination of trans-cinnamic acid is a classic example of a stereospecific reaction.]]
    2 KB (315 words) - 08:00, 11 March 2024
  • ...l compound]] that belongs to the class of [[organic compounds]] known as [[cinnamic acids]] and derivatives. These are compounds containing a [[benzene]] ring ...to a [[cinnamoyl]] group, which is a type of [[acyl group]] derived from [[cinnamic acid]]. The cinnamoyl group is attached to the amine group via an [[amide b
    2 KB (309 words) - 17:26, 6 March 2024
  • ...nine]] to [[cinnamic acid]] by the enzyme [[phenylalanine ammonia-lyase]]. Cinnamic acid is then converted to [[p-coumaric acid]] by the enzyme [[cinnamate 4-h * [[Cinnamic acid]]
    2 KB (234 words) - 01:21, 11 March 2024
  • ...ion between [[acid]]s and [[alcohol]]s. Methyl cinnamate is derived from [[cinnamic acid]], and its chemical formula is C10H10O2. Methyl cinnamate is typically produced through the [[esterification]] of cinnamic acid and [[methanol]], in the presence of a strong acid such as [[sulfuric
    2 KB (270 words) - 16:39, 27 February 2024
  • ...zation]] (MALDI) mass spectrometry. This compound is a [[derivative]] of [[cinnamic acid]] and is a common [[matrix (chemistry)|matrix]] for MALDI mass spectro * [[Cinnamic acid]]
    1 KB (190 words) - 14:27, 8 March 2024
  • ...[[enzyme]] that catalyzes the deamination of [[phenylalanine]] to [[trans-cinnamic acid]] and [[ammonia]]. This reaction is the first step in the [[phenylprop ...PAL is to catalyze the non-oxidative deamination of phenylalanine to trans-cinnamic acid and ammonia. This reaction is the first step in the phenylpropanoid pa
    2 KB (213 words) - 18:12, 29 February 2024
  • ...roxycinnamic acid]], an organic compound that is a hydroxy derivative of [[cinnamic acid]]. There are three isomers, o-coumaric acid, m-coumaric acid, and p-co * [[Cinnamic acid]]
    2 KB (220 words) - 13:22, 8 March 2024
  • ...odium salt]], [[monosodium 3-(4-hydroxy-3-methoxyphenyl)-2-propenoate]], [[cinnamic acid, 4-hydroxy-3-methoxy-, monosodium salt]], [[monosodium 4-hydroxy-3-met
    476 bytes (53 words) - 21:44, 21 March 2024
  • ...] (PAL) enzyme, which converts [[phenylalanine]] to [[cinnamic acid]]. The cinnamic acid is then converted to the phenyl group by a series of [[enzymatic react
    2 KB (227 words) - 01:15, 11 March 2024
  • ...with the conversion of [[Phenylalanine|phenylalanine]] to [[Cinnamic acid|cinnamic acid]] by the enzyme [[Phenylalanine ammonia-lyase|phenylalanine ammonia-ly
    2 KB (259 words) - 20:02, 28 February 2024
  • ...nto [[cinnamic acid]] by the enzyme [[phenylalanine ammonia lyase]] (PAL). Cinnamic acid is then converted into [[p-coumaric acid]] by [[cinnamate 4-hydroxylas
    2 KB (260 words) - 06:21, 29 February 2024
  • ...commonly found in a variety of [[plant]] species. It is a derivative of [[cinnamic acid]] and is known for its various [[biological activities]] including [[a * [[Cinnamic acid]]
    2 KB (279 words) - 03:28, 22 February 2024
  • ...way]], which involves the conversion of phenylalanine into [[Cinnamic acid|cinnamic acid]], followed by a series of enzymatic reactions.
    2 KB (282 words) - 17:10, 29 February 2024
  • Alpha-cyano-4-hydroxycinnamate is a derivative of [[cinnamic acid]], with a cyano group (-CN) at the alpha position and a hydroxy group * [[Cinnamic acid]]
    2 KB (271 words) - 06:44, 11 March 2024
  • ...nine]] to [[cinnamic acid]] by the enzyme [[phenylalanine ammonia-lyase]]. Cinnamic acid is then converted to [[p-coumaric acid]] by [[cinnamate 4-hydroxylase]
    2 KB (290 words) - 12:25, 10 March 2024
  • ...lanine ammonia-lyase catalyzes the deamination of L-phenylalanine to trans-cinnamic acid and ammonia. This reaction is an important step in the phenylpropanoid ...potential applications. The enzyme can be used in the production of trans-cinnamic acid, which has various industrial uses, including the synthesis of fragran
    2 KB (297 words) - 00:24, 22 January 2024
  • ...ne]] into [[cinnamic acid]] by the enzyme [[phenylalanine ammonia lyase]]. Cinnamic acid is then hydroxylated by [[cinnamate 4-hydroxylase]] to form [[p-coumar
    2 KB (319 words) - 22:11, 25 February 2024
  • ...ries of enzymatic reactions. This process begins with the hydroxylation of cinnamic acid, which is then followed by lactonization to form the coumarin structur * [[Cinnamic acid]]
    3 KB (459 words) - 04:10, 22 March 2024

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