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Línia 1: {{ Unreferenced .3. date =September 2007}} .. ~~{{Petició de traducció\|en\|Cadinene\|--[[Usuari:Mafoso\|Marc]] ([[Usuari Discussió:Mafoso\|Mani'm?]]) 08:05, 23 juny 2010 (CEST)}}~~ {{ chembox .. .3. Name = (+)-α-Cadinene .. .3. ImageFile = Alpha_cadinene.png .. .3. ImageSize = 135px .. .3. ImageName = α-cadinene .. .3. Iupacname = (1S ,4aR ,8aR)-4 ,7-dimethyl-1-(propan-2-yl)- .. 1 ,2 ,4a ,5 ,6 ,8a-hexahydronaphthalene .. .3. Section1 = {{ Chembox Identifiers .. }} .. .3. Section2 = {{ Chembox Properties .. .3. C = 15 .3. H = 24 .. .3. Density = .. .3. MeltingPt = .. .3. BoilingPt = .. }} .. }} .. {{ chembox .. .3. Name = &gamma ;-Cadinene .. .3. ImageFile1 = Gamma-cadinene.png .. .3. ImageSize1 = 135px .. .3. Iupacname = (1S ,4aR ,8aR)-7-methyl-4-methylidene-1- .. (propan-2-yl)-1 ,2 ,3 ,4 ,4a ,5 ,6 ,8a-octahydronaphthalene .. .3. Section1 = {{ Chembox Identifiers .. }} .. .3. Section2 = {{ Chembox Properties .. .3. C = 15 .3. H = 24 .. .3. Density = .. .3. MeltingPt = .. .3. BoilingPt = .. }} .. }} .. {{ chembox .. .3. Name = &delta ;-Cadinene .. .3. ImageFile1 = Delta cadinene.png .. .3. ImageSize1 = 135px .. .3. Iupacname = (1S ,8aR)-4 ,7-dimethyl-1-(propan-2-yl)- .. 1 ,2 ,3 ,5 ,6 ,8a-hexahydronaphthalene .. .3. Section1 = {{ Chembox Identifiers .. }} .. .3. Section2 = {{ Chembox Properties .. .3. C = 15 .3. H = 24 .. .3. Density = .. .3. MeltingPt = .. .3. BoilingPt = .. }} .. }} .. ((((( Cadinene ))))) is the trivial chemical name of a number of ISOMERIC HYDROCARBONS that occur in a wide variety of ESSENTIAL OIL-producing plants. The name is derived from that of the CADE JUNIPER ((( JUNIPERUS OXYCEDRUS )) L.) , the wood of which yields an oil from which cadinene isomers were first isolated. .. .. Chemically , the cadinenes are BICYCLIC SESQUITERPENES. The term “cadinene” has sometimes been used in a broad sense to refer to any sesquiterpene with the so-called cadalane (4-isopropyl-1 ,6-dimethyldecahydronaphthalene) carbon skeleton. Because of the large number of known double-bond and stereochemical isomers , this class of compounds has been subdivided into four subclasses based on the RELATIVE STEREOCHEMISTRY at the isopropyl group and the two BRIDGEHEAD carbon atoms. The name (( cadinene )) is now properly used only for the first subclass below , which includes the compounds originally isolated from CADE OIL. Only one ENANTIOMER of each subclass is depicted , with the understanding that the other enantiomer bears the same subclass name. .. .. <gallery perrow="3"> .. Image:Cadalane.svg .3. Cadalane skeleton .. Image:Cadinane.svg .3. Cadinene stereochemistry .. Image:Muurolane.svg .3. Muurolene stereochemistry .. Image:Amorphane.svg .3. Amorphene stereochemistry .. Image:Bulgarane.svg .3. Bulgarene stereochemistry .. </gallery> .. .. (==) References (==) .. {{ reflist}} .. .. [[Category:Flavors]] .. [[Category:Alkenes]] .. [[Category:Sesquiterpenes]] .. .. [[de:Cadinen (Verbindung)]] .. [[ru:Кадинен]] .. .. {{ hydrocarbon-stub}} .. paraulesenllacos .. .. ISOMERIC .. .. HYDROCARBONS .. .. ESSENTIAL OIL .. .. CADE JUNIPER ((( JUNIPERUS OXYCEDRUS )) L.) .. .. BICYCLIC .. .. SESQUITERPENES .. .. RELATIVE STEREOCHEMISTRY .. .. BRIDGEHEAD .. .. CADE OIL .. .. ENANTIOMER ..

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