dbo:abstract |
3,5-Dimethylpiperidines are chemical compounds with the formula C5H8(CH3)2NH. Two diastereomers exist: the achiral R,S isomer and the chiral R,R/S,S enantiomeric pair. 3,5-Dimethylpiperidine is a precursor to tibric acid. The compound is typically prepared by hydrogenation of 3,5-dimethylpyridine. Both diastereomers also arise from the reduction of 3,5-dimethylpyridine with lithium triethylborohydride. (en) |
dbo:alternativeName |
3,5-Lupetidine (en) |
dbo:iupacName |
3,5-Dimethylpiperidine (en) |
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wiki-commons:Special:FilePath/3,5-dimethylpiperidine.svg?width=300 |
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dbr:Enantiomer dbr:Lithium_triethylborohydride dbc:Piperidines dbr:Chemical_compound dbr:Chirality_(chemistry) dbr:2,6-Dimethylpiperidine dbr:Tibric_acid dbr:Piperidine dbr:Diastereomers |
dbp:imagefile |
35 (xsd:integer) |
dbp:imagename |
Structure of 3,5-dimethylpiperidine (en) |
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35 (xsd:integer) |
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35 (xsd:integer) |
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35 (xsd:integer) |
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dct:subject |
dbc:Piperidines |
gold:hypernym |
dbr:Compounds |
rdf:type |
owl:Thing dul:ChemicalObject dbo:ChemicalSubstance wikidata:Q11173 dbo:ChemicalCompound |
rdfs:comment |
3,5-Dimethylpiperidines are chemical compounds with the formula C5H8(CH3)2NH. Two diastereomers exist: the achiral R,S isomer and the chiral R,R/S,S enantiomeric pair. 3,5-Dimethylpiperidine is a precursor to tibric acid. The compound is typically prepared by hydrogenation of 3,5-dimethylpyridine. Both diastereomers also arise from the reduction of 3,5-dimethylpyridine with lithium triethylborohydride. (en) |
rdfs:label |
3,5-Dimethylpiperidine (en) |
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freebase:3,5-Dimethylpiperidine wikidata:3,5-Dimethylpiperidine dbpedia-sr:3,5-Dimethylpiperidine https://global.dbpedia.org/id/ZCLV |
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wikipedia-en:3,5-Dimethylpiperidine?oldid=984170846&ns=0 |
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3,5-Dimethylpiperidine (en) |
is dbo:wikiPageRedirects of |
dbr:3,5-Lupetidine dbr:3,5-dimethylpiperidine |
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dbr:C7H15N dbr:Dimethylpiperidine dbr:3,5-Lupetidine dbr:3,5-dimethylpiperidine |
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wikipedia-en:3,5-Dimethylpiperidine |