dbo:abstract |
4-Phenyl-3-buten-2-on (Benzylidenaceton) ist eine chemische Verbindung aus der Gruppe der Ketone. (de) Benzylideneacetone is the organic compound described by the formula C6H5CH=CHC(O)CH3. Although both cis- and trans-isomers are possible for the α,β-unsaturated ketone, only the trans isomer is observed. Its original preparation demonstrated the scope of condensation reactions to construct new, complex organic compounds. Benzylideneacetone is used as a flavouring ingredient in food and perfumes. (en) ベンジリデンアセトン (benzylideneacetone) は、化学式がC6H5CH=CHC(O)CH3の有機化合物である。α,β不飽和ケトンであるためcis体、trans体の両方の構造が可能であるが、観測されるのはtrans体のみである。 (ja) Benzylideenaceton is een organische verbinding met als brutoformule C10H10O. Hoewel in principe rond de dubbele binding cis-trans-isomerie kan bestaan, is alleen het trans-isomeer beschreven. De eerste beschrijving van deze verbinding, en zijn bereiding, in 1881, toonde duidelijk de mogelijkheden van de aldolcondensatie als manier om nieuwe koolstof-koolstofbindingen te maken. (nl) 亚苄基丙酮是一种有机化合物,分子式为C6H5CH=CHC(O)CH3。虽然从理论上该α,β-不饱和酮化合物同时存在顺反异构体,但至今只发现了其反式异构体。该化合物的最早合成方法说明了缩合反应可以合成诸多复杂的全新有机化合物。 (zh) |
dbo:alternativeName |
Benzalacetone (en) Benzylidene acetone (en) Benzylideneacetone (en) Methyl styryl ketone (en) |
dbo:iupacName |
(3E)-4-Phenylbut-3-en-2-one (en) |
dbo:thumbnail |
wiki-commons:Special:FilePath/Benzylideneacetone-2D-skeletal.png?width=300 |
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dbo:wikiPageRevisionID |
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dbo:wikiPageWikiLink |
dbr:Pyran dbr:Enolate dbr:Benzaldehyde dbr:Benzylacetone dbr:Lithium_diisopropylamide dbc:Enones dbc:Phenyl_compounds dbr:Organic_compound dbr:Cinnamaldehyde dbr:Ketone dbr:Warfarin dbr:Cis-trans_isomerism dbr:4-Hydroxycoumarin dbr:Acetone dbr:Alkenes dbr:Alpha_and_beta_carbon dbr:Hydrazone dbr:Dibenzylideneacetone dbr:Diiron_nonacarbonyl dbr:Claisen-Schmidt_condensation dbr:Enolate_ion dbr:Alpha_carbon dbr:(benzylidene)iron_tricarbonyl dbr:Diels-Alder dbr:File:LiHMDS_EnolateFormation.png |
dbp:imagefile |
Benzylideneacetone-2D-skeletal.png (en) Benzylideneacetone-3D-balls.png (en) |
dbp:name |
Benzylideneacetone (en) |
dbp:othernames |
Benzalacetone (en) Benzylidene acetone (en) Benzylideneacetone (en) Methyl styryl ketone (en) |
dbp:pin |
-4 (xsd:integer) |
dbp:verifiedrevid |
459955431 (xsd:integer) |
dbp:watchedfields |
changed (en) |
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dct:subject |
dbc:Enones dbc:Phenyl_compounds |
gold:hypernym |
dbr:Compound |
rdf:type |
owl:Thing dul:ChemicalObject dbo:ChemicalSubstance wikidata:Q11173 yago:Abstraction100002137 yago:Chemical114806838 yago:Compound114818238 yago:Ketone114926294 yago:Material114580897 yago:Matter100020827 yago:OrganicCompound114727670 yago:Part113809207 yago:PhysicalEntity100001930 yago:Relation100031921 yago:WikicatKetones dbo:ChemicalCompound yago:Substance100019613 umbel-rc:ChemicalSubstanceType |
rdfs:comment |
4-Phenyl-3-buten-2-on (Benzylidenaceton) ist eine chemische Verbindung aus der Gruppe der Ketone. (de) Benzylideneacetone is the organic compound described by the formula C6H5CH=CHC(O)CH3. Although both cis- and trans-isomers are possible for the α,β-unsaturated ketone, only the trans isomer is observed. Its original preparation demonstrated the scope of condensation reactions to construct new, complex organic compounds. Benzylideneacetone is used as a flavouring ingredient in food and perfumes. (en) ベンジリデンアセトン (benzylideneacetone) は、化学式がC6H5CH=CHC(O)CH3の有機化合物である。α,β不飽和ケトンであるためcis体、trans体の両方の構造が可能であるが、観測されるのはtrans体のみである。 (ja) Benzylideenaceton is een organische verbinding met als brutoformule C10H10O. Hoewel in principe rond de dubbele binding cis-trans-isomerie kan bestaan, is alleen het trans-isomeer beschreven. De eerste beschrijving van deze verbinding, en zijn bereiding, in 1881, toonde duidelijk de mogelijkheden van de aldolcondensatie als manier om nieuwe koolstof-koolstofbindingen te maken. (nl) 亚苄基丙酮是一种有机化合物,分子式为C6H5CH=CHC(O)CH3。虽然从理论上该α,β-不饱和酮化合物同时存在顺反异构体,但至今只发现了其反式异构体。该化合物的最早合成方法说明了缩合反应可以合成诸多复杂的全新有机化合物。 (zh) |
rdfs:label |
Benzylideneacetone (en) 4-Phenyl-3-buten-2-on (de) ベンジリデンアセトン (ja) Benzylideenaceton (nl) 亚苄基丙酮 (zh) |
owl:sameAs |
freebase:Benzylideneacetone yago-res:Benzylideneacetone wikidata:Benzylideneacetone http://azb.dbpedia.org/resource/بنزیلیدن_استون dbpedia-de:Benzylideneacetone dbpedia-fa:Benzylideneacetone dbpedia-fi:Benzylideneacetone dbpedia-ja:Benzylideneacetone dbpedia-nl:Benzylideneacetone dbpedia-sh:Benzylideneacetone dbpedia-sr:Benzylideneacetone dbpedia-zh:Benzylideneacetone https://global.dbpedia.org/id/445z1 |
prov:wasDerivedFrom |
wikipedia-en:Benzylideneacetone?oldid=1118575097&ns=0 |
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wiki-commons:Special:FilePath/Benzylideneacetone-2D-skeletal.png wiki-commons:Special:FilePath/Benzylideneacetone-3D-balls.png wiki-commons:Special:FilePath/LiHMDS_EnolateFormation.png |
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wikipedia-en:Benzylideneacetone |
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Benzylideneacetone (en) |
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dbr:BDA |
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dbr:BDA dbr:Benzylacetone dbr:C10H10O dbr:C6H5CHCHC(O)CH3 dbr:(Benzylideneacetone)iron_tricarbonyl dbr:Organocatalysis dbr:Michael_reaction dbr:Benzylidene_acetone dbr:Dibenzylideneacetone dbr:Mesityl_oxide dbr:Methyl_styryl_ketone dbr:Acetocinnamoen dbr:4-Phenyl-3-buten-2-one dbr:Benzalacetone |
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