{{chembox | verifiedrevid = 443975833 | ImageFileL1 = chrysanthenone.png | ImageSizeL1 = 100px | ImageFileR1 = chrysanthenone3D.png | ImageSizeR1 = 120px | IUPACName = 2,7,7-Trimethylbicyclo[3.1.1]hept-2-en-6-one | OtherNames = 2-Pinen-7-one | Section1 = {{Chembox Identifiers | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 390901 | ChEBI=3681 | KEGG_Ref = {{keggcite|correct|kegg}} | KEGG = C11394 | InChI = 1/C10H14O/c1-6-4-5-7-9(11)8(6)10(7,2)3/h4,7-8H,5H2,1-3H3 | InChIKey = IECBDTGWSQNQID-UHFFFAOYAO | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/C10H14O/c1-6-4-5-7-9(11)8(6)10(7,2)3/h4,7-8H,5H2,1-3H3 | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = IECBDTGWSQNQID-UHFFFAOYSA-N | CASNo_Ref = {{cascite|correct|??}} | CASNo = 473-06-3 | UNII_Ref = {{fdacite|correct|FDA}} | UNII = 841NXH6XEV | EINECS = | PubChem = 442463 | SMILES = O=C1C2/C(=C\CC1C2(C)C)C }} | Section2 = {{Chembox Properties | Formula = C<sub>10</sub>H<sub>14</sub>O | MolarMass = 150.22 g/mol | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = }} }}
'''Chrysanthenone ''' (C<sub>10</sub>H<sub>14</sub>O) is a terpenoid. It can be produced from its isomer verbenone in a photochemical rearrangement reaction.<ref>{{cite journal | last1 = Erman | first1 = William F. | journal = Journal of the American Chemical Society | volume = 89 | pages = 3828 | year = 1967 | title= Photochemical transformations of unsaturated bicyclic ketones. Verbenone and its photodynamic products of ultraviolet irradiation |doi = 10.1021/ja00991a026 | issue = 15}}</ref>
:300px|Chrysanthenone from verbenone
==References== {{reflist}}
==External links== *[http://www.pherobase.com/database/kovats/kovats-detail-chrysanthenone.php Kovats - chrysanthenone]
Category:Ketones Category:Monoterpenes Category:Cycloalkenes Category:Cyclobutanes