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Phenylcinnamic acid: Difference between revisions

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#REDIRECT ]
{{Chembox

| ImageFile = Phenylcinnamic Acid.jpeg
{{R category shell|
| ImageAlt = Skeleton Formula for Alpha-Phenylcinnamic Acid
{{R from less specific name}}
| IUPACName = (2E)-2,3-diphenylprop-2-enoic acid
{{R with history}}
| OtherNames = Alpha-Phenylcinnamic Acid, a-(Phenylmethylene)benzeneacetic acid, a-Phenyl-trans-cinnamic acid, α-Phenylcinnamic acid
| Section1 = {{Chembox Identifiers
| CASNo = 91-48-5
| SMILES = OC(=O)C(=C/C1=CC=CC=C1)/C2=CC=CC=C2}}
| Section2 = {{Chembox Properties
| Formula = C15H12O2
| MolarMass = 224.25g/mol<ref>http://www.chemicalbook.com/ProductChemicalPropertiesCB6854603_EN.htm</ref>
| Appearance = White to Light Yellow Powder
| MeltingPt = 172°C - 174°C
| BoilingPt = 224°C - 225°C
| Solubility = Slightly soluble in water}}
| Section3 = {{Chembox Hazards
| MainHazards = Irritant<ref>http://msds.chem.ox.ac.uk/PH/alpha-phenyl_cinnamic_acid.html</ref>}}
}} }}

Alpha-Phenylcinnamic Acid is a ], or, more specifically, ]. It has the formula C15H12O2 and appears as an off-white crystalline solid<ref>http://www.chemexper.com/search/cas/91485.html</ref>.

==Uses==
Alpha-Phenylcinnamic Acid is frequently used as a compound synthesized in undergraduate laboratories to study the ], but is primarily seen as in intermediate or precursor to other, more useful phenylpropanoids.

==Synthesis==
There are many ways to synthesize Alpha-Phenylcinnamic acid; some of the more popular methods of formation include the condensation of ] with ] in the presence of ], the distillation of ], or by the reaction of ] with ] in ]<ref>Organic Syntheses, Coll. Vol. 4, p.777 (1963); Vol. 33, p.70 (1953).</ref>.

==References==

{{reflist}}

]

Latest revision as of 04:55, 26 September 2024

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