http://dbpedia.org/ontology/abstract
|
3-Chloropropionitrile is an organic compou … 3-Chloropropionitrile is an organic compound with the formula ClCH2CH2CN. A colorless liquid, it is prepared by the reaction of hydrogen chloride with acrylonitrile. It is used commercially as a precursor to the drug famotidine. It is an alkylating agent, as illustrated by its reaction with imidazoles to give the cyanoethylated imidazolium salts. Similarly, it alkylates thiourea, en route to 3-mercaptopropionitrile.urea, en route to 3-mercaptopropionitrile.
|
http://dbpedia.org/ontology/alternativeName
|
1-Chloro-2-cyanoethane; β-Chloropropionitrile
|
http://dbpedia.org/ontology/iupacName
|
3-Chloropropanenitrile
|
http://dbpedia.org/ontology/thumbnail
|
http://commons.wikimedia.org/wiki/Special:FilePath/3-Chloropropionitrile.svg?width=300 +
|
http://dbpedia.org/ontology/wikiPageID
|
37267896
|
http://dbpedia.org/ontology/wikiPageLength
|
2675
|
http://dbpedia.org/ontology/wikiPageRevisionID
|
1074835808
|
http://dbpedia.org/ontology/wikiPageWikiLink
|
http://dbpedia.org/resource/Thiourea +
, http://dbpedia.org/resource/Imidazole +
, http://dbpedia.org/resource/Hydrogen_chloride +
, http://dbpedia.org/resource/Alkylating_agent +
, http://dbpedia.org/resource/Imidazolium +
, http://dbpedia.org/resource/4-Chlorobutyronitrile +
, http://dbpedia.org/resource/Acrylonitrile +
, http://dbpedia.org/resource/Category:Nitriles +
, http://dbpedia.org/resource/Propionitrile +
, http://dbpedia.org/resource/3-Mercaptopropionitrile +
, http://dbpedia.org/resource/Famotidine +
, http://dbpedia.org/resource/Organic_compound +
, http://dbpedia.org/resource/Cyanoethylation +
|
http://dbpedia.org/property/imagefile
|
3
|
http://dbpedia.org/property/imagesize
|
200
|
http://dbpedia.org/property/othernames
|
1
|
http://dbpedia.org/property/pin
|
3
|
http://dbpedia.org/property/wikiPageUsesTemplate
|
http://dbpedia.org/resource/Template:Reflist +
, http://dbpedia.org/resource/Template:P-phrases +
, http://dbpedia.org/resource/Template:Polymer-stub +
, http://dbpedia.org/resource/Template:Chembox_Identifiers +
, http://dbpedia.org/resource/Template:Chembox_Hazards +
, http://dbpedia.org/resource/Template:Chembox_Properties +
, http://dbpedia.org/resource/Template:Chembox +
, http://dbpedia.org/resource/Template:GHS_exclamation_mark +
, http://dbpedia.org/resource/Template:Fdacite +
, http://dbpedia.org/resource/Template:Cascite +
, http://dbpedia.org/resource/Template:Chembox_Related +
, http://dbpedia.org/resource/Template:GHS_skull_and_crossbones +
, http://dbpedia.org/resource/Template:H-phrases +
|
http://purl.org/dc/terms/subject
|
http://dbpedia.org/resource/Category:Nitriles +
|
http://purl.org/linguistics/gold/hypernym
|
http://dbpedia.org/resource/Compound +
|
http://www.w3.org/ns/prov#wasDerivedFrom
|
http://en.wikipedia.org/wiki/3-Chloropropionitrile?oldid=1074835808&ns=0 +
|
http://xmlns.com/foaf/0.1/depiction
|
http://commons.wikimedia.org/wiki/Special:FilePath/3-Chloropropionitrile.svg +
|
http://xmlns.com/foaf/0.1/isPrimaryTopicOf
|
http://en.wikipedia.org/wiki/3-Chloropropionitrile +
|
owl:sameAs |
https://global.dbpedia.org/id/4JUHY +
, http://yago-knowledge.org/resource/3-Chloropropionitrile +
, http://www.wikidata.org/entity/Q4634123 +
, http://sr.dbpedia.org/resource/3-Hloropropionitril +
, http://dbpedia.org/resource/3-Chloropropionitrile +
, http://ta.dbpedia.org/resource/3-%E0%AE%95%E0%AF%81%E0%AE%B3%E0%AF%8B%E0%AE%B0%E0%AF%8B%E0%AE%AA%E0%AF%81%E0%AE%B0%E0%AF%8B%E0%AE%AA%E0%AF%8D%E0%AE%AA%E0%AE%BF%E0%AE%AF%E0%AF%8B%E0%AE%A8%E0%AF%88%E0%AE%9F%E0%AF%8D%E0%AE%B0%E0%AF%88%E0%AE%B2%E0%AF%8D +
, http://sh.dbpedia.org/resource/3-Hloropropionitril +
, http://rdf.freebase.com/ns/m.0n5x78w +
|
rdf:type |
http://dbpedia.org/class/yago/Message106598915 +
, http://www.ontologydesignpatterns.org/ont/dul/DUL.owl#ChemicalObject +
, http://dbpedia.org/class/yago/Abstraction100002137 +
, http://dbpedia.org/class/yago/Nitrile114827346 +
, http://dbpedia.org/class/yago/WikicatNitriles +
, http://dbpedia.org/class/yago/PhysicalEntity100001930 +
, http://dbpedia.org/class/yago/Part113809207 +
, http://dbpedia.org/class/yago/Relation100031921 +
, http://dbpedia.org/ontology/ChemicalSubstance +
, http://dbpedia.org/class/yago/Communication100033020 +
, http://dbpedia.org/class/yago/WikicatMolecularFormulas +
, http://dbpedia.org/class/yago/Matter100020827 +
, http://dbpedia.org/class/yago/OrganicCompound114727670 +
, http://dbpedia.org/class/yago/Material114580897 +
, http://dbpedia.org/class/yago/MolecularFormula106817173 +
, http://dbpedia.org/class/yago/Formula106816935 +
, http://www.wikidata.org/entity/Q11173 +
, http://dbpedia.org/class/yago/Compound114818238 +
, http://dbpedia.org/class/yago/Chemical114806838 +
, http://dbpedia.org/class/yago/Substance100019613 +
, http://dbpedia.org/ontology/ChemicalCompound +
, http://dbpedia.org/class/yago/Statement106722453 +
|
rdfs:comment |
3-Chloropropionitrile is an organic compou … 3-Chloropropionitrile is an organic compound with the formula ClCH2CH2CN. A colorless liquid, it is prepared by the reaction of hydrogen chloride with acrylonitrile. It is used commercially as a precursor to the drug famotidine. It is an alkylating agent, as illustrated by its reaction with imidazoles to give the cyanoethylated imidazolium salts. Similarly, it alkylates thiourea, en route to 3-mercaptopropionitrile.urea, en route to 3-mercaptopropionitrile.
|
rdfs:label |
3-Chloropropionitrile
|