@prefix dbo: .
@prefix dbr: .
dbr:Glycerol dbo:wikiPageWikiLink dbr:Solketal .
@prefix foaf: .
@prefix wikipedia-en: .
wikipedia-en:Solketal foaf:primaryTopic dbr:Solketal .
dbr:Acetonide dbo:wikiPageWikiLink dbr:Solketal .
dbr:C6H12O3 dbo:wikiPageWikiLink dbr:Solketal .
@prefix rdf: .
@prefix yago: .
dbr:Solketal rdf:type yago:Fluid114939900 .
@prefix ns6: .
dbr:Solketal rdf:type ns6:ChemicalObject ,
yago:CausalAgent100007347 ,
dbo:ChemicalCompound ,
yago:Matter100020827 .
@prefix wikidata: .
dbr:Solketal rdf:type wikidata:Q11173 ,
yago:Substance100019613 ,
yago:Agent114778436 ,
yago:DrugOfAbuse103248958 ,
yago:Part113809207 ,
yago:Drug103247620 ,
yago:PhysicalEntity100001930 ,
yago:Beverage107881800 ,
yago:Relation100031921 ,
yago:Liquid114940386 ,
yago:Food100021265 ,
yago:Substance100020090 ,
dbo:ChemicalSubstance ,
yago:WikicatPrimaryAlcohols ,
yago:Abstraction100002137 ,
yago:WikicatAlcohols ,
yago:Alcohol107884567 .
@prefix owl: .
dbr:Solketal rdf:type owl:Thing .
@prefix rdfs: .
dbr:Solketal rdfs:label "Solketal"@en ,
"Glycerolaceton"@nl ,
"Isopropylidenglycerin"@de ,
"Solketal"@cs ;
rdfs:comment "Solketal je chr\u00E1n\u011Bn\u00E1 forma glycerolu s isopropylidenacetalovou skupinou spojuj\u00EDc\u00ED dva sousedn\u00ED hydroxyly. Solketal m\u00E1 na prost\u0159edn\u00EDm uhl\u00EDku glycerolov\u00E9ho \u0159et\u011Bzce a tak m\u016F\u017Ee b\u00FDt pou\u017E\u00EDv\u00E1n jak jako racemick\u00E1 sm\u011Bs, tak i jako jeden ze dvou enantiomer\u016F. Vyu\u017E\u00EDv\u00E1 se p\u0159i synt\u00E9z\u00E1ch mono-, di- a triglycerid\u016F. Volnou hydroxylovou skupinu solketalu lze esterifikovat karboxylov\u00FDmi kyselinami za vzniku chr\u00E1n\u011Bn\u00FDch monoglycerid\u016F, p\u0159i\u010Dem\u017E isopropylenov\u00E1 skupina m\u016F\u017Ee b\u00FDt odstran\u011Bna kyselou hydrol\u00FDzou ve vodn\u00E9m nebo alkoholov\u00E9m prost\u0159ed\u00ED. Nechr\u00E1n\u011Bn\u00FD diol lze pot\u00E9 d\u00E1le esterifikovat za tvorby di- nebo triglyceridu."@cs ,
"Isopropylidenglycerin, auch Solketal, ist eine chemische Verbindung aus der Gruppe der und der . Das Derivat des Glycerins mit einer Isopropyliden-Schutzgruppe ist bei Raumtemperatur fl\u00FCssig."@de ,
"Solketal is a protected form of glycerol with an isopropylidene acetal group joining two neighboring hydroxyl groups. Solketal contains a chiral center on the center carbon of the glycerol backbone, and so can be purchased as either the racemate or as one of the two enantiomers. Solketal has been used extensively in the synthesis of mono-, di- and triglycerides by ester bond formation. The free hydroxyl groups of solketal can be esterified with a carboxylic acid to form the protected monoglyceride, where the isopropylene group can then be removed using an acid catalyst in aqueous or alcoholic medium. The unprotected diol can then be esterified further to form either the di- or triglyceride."@en ,
"Glycerolaceton (ook isopropylideenglycerol genoemd) is een cyclische organische verbinding met als brutoformule C6H12O3. Het is een kleurloze en reukloze olieachtige vloeistof, die mengbaar is met water. De molecule bezit een chiraal centrum: het koolstofatoom in de dioxolaanring, dat zich aan de vertakking naar de OH-groep bevindt."@nl ;
foaf:depiction .
@prefix dcterms: .
@prefix dbc: .
dbr:Solketal dcterms:subject dbc:Ketals ,
dbc:Primary_alcohols ;
dbo:abstract "Isopropylidenglycerin, auch Solketal, ist eine chemische Verbindung aus der Gruppe der und der . Das Derivat des Glycerins mit einer Isopropyliden-Schutzgruppe ist bei Raumtemperatur fl\u00FCssig."@de ,
"Solketal je chr\u00E1n\u011Bn\u00E1 forma glycerolu s isopropylidenacetalovou skupinou spojuj\u00EDc\u00ED dva sousedn\u00ED hydroxyly. Solketal m\u00E1 na prost\u0159edn\u00EDm uhl\u00EDku glycerolov\u00E9ho \u0159et\u011Bzce a tak m\u016F\u017Ee b\u00FDt pou\u017E\u00EDv\u00E1n jak jako racemick\u00E1 sm\u011Bs, tak i jako jeden ze dvou enantiomer\u016F. Vyu\u017E\u00EDv\u00E1 se p\u0159i synt\u00E9z\u00E1ch mono-, di- a triglycerid\u016F. Volnou hydroxylovou skupinu solketalu lze esterifikovat karboxylov\u00FDmi kyselinami za vzniku chr\u00E1n\u011Bn\u00FDch monoglycerid\u016F, p\u0159i\u010Dem\u017E isopropylenov\u00E1 skupina m\u016F\u017Ee b\u00FDt odstran\u011Bna kyselou hydrol\u00FDzou ve vodn\u00E9m nebo alkoholov\u00E9m prost\u0159ed\u00ED. Nechr\u00E1n\u011Bn\u00FD diol lze pot\u00E9 d\u00E1le esterifikovat za tvorby di- nebo triglyceridu."@cs ,
"Solketal is a protected form of glycerol with an isopropylidene acetal group joining two neighboring hydroxyl groups. Solketal contains a chiral center on the center carbon of the glycerol backbone, and so can be purchased as either the racemate or as one of the two enantiomers. Solketal has been used extensively in the synthesis of mono-, di- and triglycerides by ester bond formation. The free hydroxyl groups of solketal can be esterified with a carboxylic acid to form the protected monoglyceride, where the isopropylene group can then be removed using an acid catalyst in aqueous or alcoholic medium. The unprotected diol can then be esterified further to form either the di- or triglyceride."@en ,
"Glycerolaceton (ook isopropylideenglycerol genoemd) is een cyclische organische verbinding met als brutoformule C6H12O3. Het is een kleurloze en reukloze olieachtige vloeistof, die mengbaar is met water. De molecule bezit een chiraal centrum: het koolstofatoom in de dioxolaanring, dat zich aan de vertakking naar de OH-groep bevindt."@nl ;
dbo:wikiPageWikiLink dbr:Glycerol ,
dbr:Isopropylidene_acetal ,
dbr:Esterified ,
dbc:Ketals ,
dbr:Glyceride ,
dbr:Diol ,
dbr:Racemate ,
dbr:Enantiomer ,
dbc:Primary_alcohols ,
dbr:Hydroxyl .
@prefix dbp: .
@prefix dbt: .
dbr:Solketal dbp:wikiPageUsesTemplate dbt:Chemboximage ,
dbt:Fdacite ,
dbt:OrgSynth ,
dbt:Cite_journal ,
dbt:Nofootnotes ,
dbt:Cascite ,
dbt:Chemspidercite ,
dbt:Cite_web ,
dbt:Chembox_Identifiers ,
dbt:Chembox_Hazards ,
dbt:Chembox_Properties ,
dbt:Stdinchicite ,
dbt:Chembox ;
dbo:thumbnail ;
dbo:wikiPageRevisionID 1094214827 ;
dbo:wikiPageExternalLink ,
.
@prefix xsd: .
dbr:Solketal dbo:wikiPageLength "3495"^^xsd:nonNegativeInteger ;
dbo:wikiPageID 4390618 ;
dbp:title "dl-ISOPROPYLIDENEGLYCEROL"@en ;
owl:sameAs .
@prefix dbpedia-de: .
dbr:Solketal owl:sameAs dbpedia-de:Isopropylidenglycerin ,
.
@prefix dbpedia-sh: .
dbr:Solketal owl:sameAs dbpedia-sh:Solketal .
@prefix yago-res: .
dbr:Solketal owl:sameAs yago-res:Solketal ,
.
@prefix dbpedia-nl: .
dbr:Solketal owl:sameAs dbpedia-nl:Glycerolaceton .
@prefix dbpedia-cs: .
dbr:Solketal owl:sameAs dbpedia-cs:Solketal ,
.
@prefix dbpedia-sr: .
dbr:Solketal owl:sameAs dbpedia-sr:Solketal ,
,
dbr:Solketal ,
wikidata:Q2968854 .
@prefix gold: .
dbr:Solketal gold:hypernym dbr:Form .
@prefix prov: .
dbr:Solketal prov:wasDerivedFrom ;
foaf:isPrimaryTopicOf wikipedia-en:Solketal ;
dbp:othernames "Isopropylidene glycerol"@en ;
dbo:iupacName "(2,2-Dimethyl-1,3-dioxolan-4-yl)methanol"@en ;
dbp:verifiedfields "changed"@en ;
dbo:alternativeName "Isopropylidene glycerol"@en ;
dbp:verifiedrevid 402674700 ;
dbp:watchedfields "changed"@en ;
dbp:year 1955 ;
dbp:imagesize 150 ;
dbp:pin "methanol"@en ;
dbp:imagefile "Solketal.png"@en ;
dbp:collvolpages 502 ;
dbp:author "Mary Renoll and Melvin S. Newman"@en ;
dbp:collvol 3 ;
dbp:pages 73 ;
dbp:volume 28 .
dbr:Isopropylidene_glycerol dbo:wikiPageWikiLink dbr:Solketal ;
dbo:wikiPageRedirects dbr:Solketal .