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- 2-Naphthylamine abstract "2-Naphthylamine is an aromatic amine. It is used to make azo dyes. It is a known human carcinogen and has largely been replaced by less toxic compounds. 2-Naphthylamine is prepared by heating 2-naphthol with ammonium zinc chloride to 200-210 °C; or in the form of its acetyl derivative by heating 2-naphthol with ammonium acetate to 270-280 °C. It forms odorless, colorless plates which melt at 111-112 °C. It gives no color with ferric chloride. When reduced by sodium in boiling amyl alcohol solution it forms alicyclic tetrahydro-3-naphthylamine, which has most of the properties of the aliphatic amines; it is strongly alkaline in reaction, has an ammoniacal odor and cannot be diazotized. On oxidation it yields ortho-carboxy-hydrocinnamic acid, HO2CC6H4CH2CH2CO2H. Numerous sulfonic acidsderived from 2-naphthylamine are known. Of these, the δ-acid and Bronner's acid are of more value technically, since they combine with ortho-tetrazoditolyl to produce fine red dye-stuffs.".
- 2-Naphthylamine iupacName "2-Aminonaphthalene".
- 2-Naphthylamine thumbnail 2-Naphthylamine.PNG?width=300.
- 2-Naphthylamine wikiPageID "5828334".
- 2-Naphthylamine wikiPageLength "3515".
- 2-Naphthylamine wikiPageOutDegree "31".
- 2-Naphthylamine wikiPageRevisionID "668310894".
- 2-Naphthylamine wikiPageWikiLink 1,8-Bis(dimethylamino)naphthalene.
- 2-Naphthylamine wikiPageWikiLink 1-Naphthylamine.
- 2-Naphthylamine wikiPageWikiLink 2-Naphthol.
- 2-Naphthylamine wikiPageWikiLink 2-naphthol.
- 2-Naphthylamine wikiPageWikiLink Acetate.
- 2-Naphthylamine wikiPageWikiLink Acetyl.
- 2-Naphthylamine wikiPageWikiLink Aliphatic_compound.
- 2-Naphthylamine wikiPageWikiLink Alkaline.
- 2-Naphthylamine wikiPageWikiLink Alkalinity.
- 2-Naphthylamine wikiPageWikiLink Amine.
- 2-Naphthylamine wikiPageWikiLink Ammonia.
- 2-Naphthylamine wikiPageWikiLink Ammonium.
- 2-Naphthylamine wikiPageWikiLink Amyl_alcohol.
- 2-Naphthylamine wikiPageWikiLink Aromatic.
- 2-Naphthylamine wikiPageWikiLink Aromaticity.
- 2-Naphthylamine wikiPageWikiLink Azo_compound.
- 2-Naphthylamine wikiPageWikiLink Azo_dyes.
- 2-Naphthylamine wikiPageWikiLink Bladder_cancer.
- 2-Naphthylamine wikiPageWikiLink Carcinogen.
- 2-Naphthylamine wikiPageWikiLink Category:IARC_Group_1_carcinogens.
- 2-Naphthylamine wikiPageWikiLink Category:Naphthylamines.
- 2-Naphthylamine wikiPageWikiLink Cigarette.
- 2-Naphthylamine wikiPageWikiLink Diazo.
- 2-Naphthylamine wikiPageWikiLink Ferric_chloride.
- 2-Naphthylamine wikiPageWikiLink Glucuronic_acid.
- 2-Naphthylamine wikiPageWikiLink Glucuronidase.
- 2-Naphthylamine wikiPageWikiLink Iron(III)_chloride.
- 2-Naphthylamine wikiPageWikiLink Naphthalene.
- 2-Naphthylamine wikiPageWikiLink Naphthol.
- 2-Naphthylamine wikiPageWikiLink Oxidation.
- 2-Naphthylamine wikiPageWikiLink Redox.
- 2-Naphthylamine wikiPageWikiLink Sodium.
- 2-Naphthylamine wikiPageWikiLink Sulfonic_acid.
- 2-Naphthylamine wikiPageWikiLink Zinc_chloride.
- 2-Naphthylamine wikiPageWikiLinkText "2-Naphthylamine".
- 2-Naphthylamine wikiPageWikiLinkText "2-naphthylamine".
- 2-Naphthylamine wikiPageWikiLinkText "β-Naphthylamine".
- 2-Naphthylamine hasPhotoCollection 2-Naphthylamine.
- 2-Naphthylamine imagefile "2".
- 2-Naphthylamine imagename "Ball-and-stick model".
- 2-Naphthylamine imagename "Skeletal formula".
- 2-Naphthylamine imagesize "200".
- 2-Naphthylamine iupacname "2".
- 2-Naphthylamine name "2".
- 2-Naphthylamine othernames "2".
- 2-Naphthylamine othernames "β-Naphthylamine".
- 2-Naphthylamine verifiedrevid "477214767".
- 2-Naphthylamine watchedfields "changed".
- 2-Naphthylamine wikiPageUsesTemplate Template:Chembox.
- 2-Naphthylamine subject Category:IARC_Group_1_carcinogens.
- 2-Naphthylamine subject Category:Naphthylamines.
- 2-Naphthylamine hypernym Amine.
- 2-Naphthylamine type Article.
- 2-Naphthylamine type ChemicalCompound.
- 2-Naphthylamine type ChemicalSubstance.
- 2-Naphthylamine type Article.
- 2-Naphthylamine type ChemicalObject.
- 2-Naphthylamine type Thing.
- 2-Naphthylamine type Q11173.
- 2-Naphthylamine comment "2-Naphthylamine is an aromatic amine. It is used to make azo dyes. It is a known human carcinogen and has largely been replaced by less toxic compounds. 2-Naphthylamine is prepared by heating 2-naphthol with ammonium zinc chloride to 200-210 °C; or in the form of its acetyl derivative by heating 2-naphthol with ammonium acetate to 270-280 °C. It forms odorless, colorless plates which melt at 111-112 °C. It gives no color with ferric chloride.".
- 2-Naphthylamine label "2-Naphthylamine".
- 2-Naphthylamine sameAs 2-Naphthylamin.
- 2-Naphthylamine sameAs ۲-نفتیلآمین.
- 2-Naphthylamine sameAs 2-naftyyliamiini.
- 2-Naphthylamine sameAs Bêta-Naphtylamine.
- 2-Naphthylamine sameAs 2-ナフチルアミン.
- 2-Naphthylamine sameAs 2-naftylamine.
- 2-Naphthylamine sameAs 2-Naftyloamina.
- 2-Naphthylamine sameAs 2-Naftilamina.
- 2-Naphthylamine sameAs m.0f7t8c.
- 2-Naphthylamine sameAs 2-Naftilamin.
- 2-Naphthylamine sameAs 2-Naftilamin.
- 2-Naphthylamine sameAs Q209450.
- 2-Naphthylamine sameAs Q209450.
- 2-Naphthylamine wasDerivedFrom 2-Naphthylamine?oldid=668310894.
- 2-Naphthylamine depiction 2-Naphthylamine.PNG.
- 2-Naphthylamine isPrimaryTopicOf 2-Naphthylamine.
- 2-Naphthylamine name "2-Naphthylamine".