Chrysanthenone: Difference between revisions
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| verifiedrevid = |
| verifiedrevid = 443975833 |
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| ImageFileL1 = chrysanthenone.png |
| ImageFileL1 = chrysanthenone.png |
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| ImageSizeL1 = 100px |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 390901 |
| ChemSpiderID = 390901 |
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| ChEBI=3681 |
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| KEGG_Ref = {{keggcite|correct|kegg}} |
| KEGG_Ref = {{keggcite|correct|kegg}} |
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| KEGG = C11394 |
| KEGG = C11394 |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey = IECBDTGWSQNQID-UHFFFAOYSA-N |
| StdInChIKey = IECBDTGWSQNQID-UHFFFAOYSA-N |
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| CASNo_Ref = {{cascite|correct|??}} |
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| CASNo = 473-06-3 |
| CASNo = 473-06-3 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = 841NXH6XEV |
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| EINECS = |
| EINECS = |
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| PubChem = 442463 |
| PubChem = 442463 |
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'''Chrysanthenone ''' (C<sub>10</sub>H<sub>14</sub>O) is a [[ |
'''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> |
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[[Image:Chrysanthenone synthesis.png|300px|Chrysanthenone from verbenone]] |
:[[Image:Chrysanthenone synthesis.png|300px|Chrysanthenone from verbenone]] |
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==References== |
==References== |
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[[Category:Ketones]] |
[[Category:Ketones]] |
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[[Category:Monoterpenes]] |
[[Category:Monoterpenes]] |
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[[Category:Cycloalkenes]] |
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[[Category:Cyclobutanes]] |
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