2,2,4,4-Tetramethyl-1,3-cyclobutanediol (original) (raw)
2,2,4,4-Tetramethyl-1,3-cyclobutanediol (CBDO) is an aliphatic diol. This diol is produced as a mixture of cis- and trans-isomers, depending on the relative stereochemistry of the hydroxyl groups. It is used as a monomer for the synthesis of polymeric materials. CBDO is currently being researched as an alternative to bisphenol A (BPA). BPA is a precursor used in the production of a wide range of polymers including polycarbonates, polyesters, polysulfones, and polyester ketones.
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| dbo:abstract | 2,2,4,4-Tetramethyl-1,3-cyclobutanediol (CBDO) is an aliphatic diol. This diol is produced as a mixture of cis- and trans-isomers, depending on the relative stereochemistry of the hydroxyl groups. It is used as a monomer for the synthesis of polymeric materials. CBDO is currently being researched as an alternative to bisphenol A (BPA). BPA is a precursor used in the production of a wide range of polymers including polycarbonates, polyesters, polysulfones, and polyester ketones. (en) 2,2,4,4-Tetramethylcyclobutan-1,3-diol ist eine chemische Verbindung aus der Gruppe der Diole. Sie kommt in zwei isomeren Formen vor, der cis-Form und der trans-Form. (de) El 2,2,4,4-tetrametil-1,3-ciclobutanodiol es un diol alifático de fórmula molecular C8H16O2.Su estructura comprende un anillo de ciclobutano con dos grupos hidroxilo (-OH) en los extremos opuestos del mismo (posiciones 1 y 3). Unidos a cada una de las dos posiciones restantes (2 y 4) hay dos grupos metilo (-CH3).Los carbonos de las posiciones 1 y 3 del anillo son asimétricos, lo que convierte al 2,2,4,4-tetrametil-1,3-ciclobutanodiol en una molécula quiral con dos esteroisómeros, cis y trans. (es) 2,2,4,4-Tetramethyl-1,3-cyclobutaandiol (CBDO) is een alicyclisch diol. Er bestaat een trans- en een cis-stereo-isomeer van, met een verschillende ruimtelijke oriëntatie van de twee hydroxylgroepen. Het technisch product is een mengsel van de twee stereo-isomeren. (nl) |
| dbo:alternativeName | 1,1,3,3-Tetramethyl-2,4-cyclobutanediol (en) |
| dbo:iupacName | 2,2,4,4-Tetramethylcyclobutane-1,3-diol (en) |
| dbo:thumbnail | wiki-commons:Special:FilePath/CBDO.png?width=300 |
| dbo:wikiPageExternalLink | http://fscimage.fishersci.com/msds/04302.htm |
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| dbo:wikiPageLength | 6821 (xsd:nonNegativeInteger) |
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| dbo:wikiPageWikiLink | dbr:Endocrine_disruptor dbr:Bisphenol_A dbr:Rhodium dbr:Ruthenium dbc:Diols dbc:Monomers dbr:Ketene dbr:Ketone dbr:Polysulfone dbr:2,2,4,4-Tetramethylcyclobutanedione dbr:Cis-trans_isomerism dbr:Nickel dbr:Diol dbr:Isomer dbc:Cyclobutanes dbr:Isobutyric_acid dbr:Hydrogenation dbr:Polycarbonate dbr:Polymer dbr:Catalysts dbr:File:CBDO_Reaction_Scheme.png |
| dbp:imagealtl | Trans CBDO molecule (en) |
| dbp:imagealtr | Cis CBDO molecule (en) |
| dbp:imagecaption | cis- and trans-2,2,4,4-Tetramethyl-1,3-cyclobutanediol (en) |
| dbp:imagefile | CBDO.png (en) |
| dbp:imagefilel | -CBDO-3D-balls.png (en) |
| dbp:imagefiler | -CBDO-3D-balls.png (en) |
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| dct:subject | dbc:Diols dbc:Monomers dbc:Cyclobutanes |
| gold:hypernym | dbr:Diol |
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| rdfs:comment | 2,2,4,4-Tetramethyl-1,3-cyclobutanediol (CBDO) is an aliphatic diol. This diol is produced as a mixture of cis- and trans-isomers, depending on the relative stereochemistry of the hydroxyl groups. It is used as a monomer for the synthesis of polymeric materials. CBDO is currently being researched as an alternative to bisphenol A (BPA). BPA is a precursor used in the production of a wide range of polymers including polycarbonates, polyesters, polysulfones, and polyester ketones. (en) 2,2,4,4-Tetramethylcyclobutan-1,3-diol ist eine chemische Verbindung aus der Gruppe der Diole. Sie kommt in zwei isomeren Formen vor, der cis-Form und der trans-Form. (de) El 2,2,4,4-tetrametil-1,3-ciclobutanodiol es un diol alifático de fórmula molecular C8H16O2.Su estructura comprende un anillo de ciclobutano con dos grupos hidroxilo (-OH) en los extremos opuestos del mismo (posiciones 1 y 3). Unidos a cada una de las dos posiciones restantes (2 y 4) hay dos grupos metilo (-CH3).Los carbonos de las posiciones 1 y 3 del anillo son asimétricos, lo que convierte al 2,2,4,4-tetrametil-1,3-ciclobutanodiol en una molécula quiral con dos esteroisómeros, cis y trans. (es) 2,2,4,4-Tetramethyl-1,3-cyclobutaandiol (CBDO) is een alicyclisch diol. Er bestaat een trans- en een cis-stereo-isomeer van, met een verschillende ruimtelijke oriëntatie van de twee hydroxylgroepen. Het technisch product is een mengsel van de twee stereo-isomeren. (nl) |
| rdfs:label | 2,2,4,4-Tetramethyl-1,3-cyclobutandiol (de) 2,2,4,4-Tetramethyl-1,3-cyclobutanediol (en) 2,2,4,4-tetrametil-1,3-ciclobutanodiol (es) 2,2,4,4-tetramethyl-1,3-cyclobutaandiol (nl) |
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| prov:wasDerivedFrom | wikipedia-en:2,2,4,4-Tetramethyl-1,3-cyclobutanediol?oldid=1118576650&ns=0 |
| foaf:depiction | wiki-commons:Special:FilePath/(E)-CBDO-3D-balls.png wiki-commons:Special:FilePath/(Z)-CBDO-3D-balls.png wiki-commons:Special:FilePath/CBDO.png wiki-commons:Special:FilePath/CBDO_Reaction_Scheme.png |
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| is dbo:wikiPageWikiLink of | dbr:Bisphenol_A dbr:C8H16O2 dbr:CBDO dbr:2,2,4,4-Tetramethylcyclobutanedione dbr:2,2,4,4-tetramethyl-1,3-cyclobutanediol dbr:Nalgene dbr:Tetramethylcyclobutanediol |
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