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Statements

Subject Item
dbr:BSTFA
rdf:type
yago:Abstraction100002137 yago:Idea105833840 dbo:ChemicalCompound yago:Acetamide114711197 yago:WikicatOrganosiliconCompounds yago:Content105809192 yago:Concept105835747 yago:PhysicalEntity100001930 wikidata:Q11173 yago:Material114580897 yago:Matter100020827 yago:Substance100019613 yago:Chemical114806838 yago:Relation100031921 yago:Whole105869584 yago:Compound114818238 yago:Amide114724264 yago:Compound105870180 n20:ChemicalObject yago:Cognition100023271 yago:WikicatFluorides yago:Halide114904359 owl:Thing yago:PsychologicalFeature100023100 yago:Fluoride114871601 dbo:ChemicalSubstance yago:WikicatAcetamides yago:OrganicCompound114727670 yago:Salt115010703 yago:Part113809207
rdfs:label
N,O-Bis(triméthylsilyl)trifluoroacétamide BSTFA
rdfs:comment
N,O-Bis(trimethylsilyl)trifluoroacetamide (BSTFA) is a chemical compound that is used to derivatise labile groups such as hydroxyl on other chemicals, with the more stable trimethylsilyl group, which protects the labile group and allows the compound to be used for analytical purposes or as a chemical reagent for synthesis of more complex molecules. Siloxanes are usually more volatile than the corresponding hydroxyl compounds, and thus can be analyzed with gas chromatography better than the parent compound. Le N,O-bis(triméthylsilyl)trifluoroacétamide (BSTFA) est un composé chimique de formule semi-développée (CH3)3Si–N=C(CF3)–O–Si(CH3)3. Il est utilisé en chimie organique pour lier un groupe triméthylsilyle –Si(CH3)3 sur un groupe fonctionnel labile afin de protéger ce dernier lors de réactions d'analyse ou de synthèse ultérieures.
foaf:name
BSTFA
dbp:name
BSTFA
foaf:depiction
n9:BSTFA-2D-skeletal-abbreviated.png n9:BSTFA-based-on-similar-xtals-3D-balls.png
dcterms:subject
dbc:Trimethylsilyl_compounds
dbo:wikiPageID
31987138
dbo:wikiPageRevisionID
838820598
dbo:wikiPageWikiLink
dbr:Gas_chromatography dbc:Trimethylsilyl_compounds dbr:Trimethylsilyl dbr:Hydroxyl
owl:sameAs
dbpedia-sr:BSTFA n16:K38E dbpedia-sh:BSTFA dbpedia-fr:N,O-Bis(triméthylsilyl)trifluoroacétamide wikidata:Q1281115 yago-res:BSTFA freebase:m.0gvr6r7 wikidata:Q114829535
dbp:wikiPageUsesTemplate
dbt:Cascite dbt:Chemspidercite dbt:Stdinchicite dbt:Chembox_Properties dbt:Chembox_Identifiers dbt:Chembox dbt:Ebicite
dbo:thumbnail
n9:BSTFA-2D-skeletal-abbreviated.png?width=300
dbp:imagealtl
Skeletal formula of BSTFA
dbp:imagealtr
Ball-and-stick model of the BSTFA molecule
dbp:imagefilel
BSTFA-2D-skeletal-abbreviated.png
dbp:imagefiler
BSTFA-based-on-similar-xtals-3D-balls.png
dbp:imagesizel
120
dbp:imagesizer
120
dbp:iupacname
trimethylsilyl 2,2,2-trifluoro-N-trimethylsilylethanimidate
dbp:othernames
BSTFA, N,O-Bistrifluoroacetamide
dbp:verifiedfields
changed
dbp:verifiedrevid
453517835
dbp:watchedfields
changed
dbo:abstract
Le N,O-bis(triméthylsilyl)trifluoroacétamide (BSTFA) est un composé chimique de formule semi-développée (CH3)3Si–N=C(CF3)–O–Si(CH3)3. Il est utilisé en chimie organique pour lier un groupe triméthylsilyle –Si(CH3)3 sur un groupe fonctionnel labile afin de protéger ce dernier lors de réactions d'analyse ou de synthèse ultérieures. N,O-Bis(trimethylsilyl)trifluoroacetamide (BSTFA) is a chemical compound that is used to derivatise labile groups such as hydroxyl on other chemicals, with the more stable trimethylsilyl group, which protects the labile group and allows the compound to be used for analytical purposes or as a chemical reagent for synthesis of more complex molecules. Siloxanes are usually more volatile than the corresponding hydroxyl compounds, and thus can be analyzed with gas chromatography better than the parent compound.
gold:hypernym
dbr:Compound
prov:wasDerivedFrom
wikipedia-en:BSTFA?oldid=838820598&ns=0
dbo:wikiPageLength
2193
dbo:alternativeName
BSTFA, N,O-Bis(trimethylsilyl)trifluoroacetamide
dbo:iupacName
trimethylsilyl 2,2,2-trifluoro-N-trimethylsilylethanimidate
foaf:isPrimaryTopicOf
wikipedia-en:BSTFA