Cyameluric acid (original) (raw)

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Cyameluric acid or 2,5,8-trihydroxy-s-heptazine is a chemical compound with formula C6N7O3H3, usually described as a heptazine molecule with the hydrogen atoms replaced by hydroxyl groups –OH; or any of its tautomers. The substance exists as an equilibrium of 17 tautomers that easily interconvert among each other. Calculations show that the symmetric tri-oxo form (1,4,7-trihydro-2,5,8-trioxo-s-heptazine) is the most stable. Therefore, this compound contains amide groups rather than imidic acids.

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dbo:abstract Cyameluric acid or 2,5,8-trihydroxy-s-heptazine is a chemical compound with formula C6N7O3H3, usually described as a heptazine molecule with the hydrogen atoms replaced by hydroxyl groups –OH; or any of its tautomers. The substance exists as an equilibrium of 17 tautomers that easily interconvert among each other. Calculations show that the symmetric tri-oxo form (1,4,7-trihydro-2,5,8-trioxo-s-heptazine) is the most stable. Therefore, this compound contains amide groups rather than imidic acids. (en)
dbo:alternativeName 1,3,4,6,7,9,9b-Heptaazaphenalene-2,5,8(1H,3H,6H)-trione; 2,5,8-trihydroxy-s-heptazine; 1,4,7-trihydro-2,5,8-trioxo-s-heptazine (en)
dbo:iupacName 2,4,6,8,10,12,13-heptazatricyclo[7.3.1.05,13]trideca-1,4,8-triene-3,7,11-trione (en)
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dbo:wikiPageWikiLink dbr:Calorie dbr:Potassium_ferrocyanide dbr:Potassium_thiocyanate dbr:Mole_(unit) dbr:Melam dbr:Hydrogen dbr:Cyclophane dbc:Heterocyclic_compounds_with_3_rings dbc:Nitrogen_heterocycles dbc:Tricyclic_compounds dbc:Triketones dbr:Melamine dbr:Melem dbr:Melon_(chemistry) dbr:Antimony_trichloride dbr:Leopold_Gmelin dbr:Linus_Pauling dbr:Functional_group dbr:Amide dbr:Cyameluric_tricyanamide dbc:Lactims dbr:Heptazine dbr:J._H._Sturdivant dbc:Amides dbr:Johann_Josef_Loschmidt dbr:Justus_von_Liebig dbr:Sulfur dbr:Hydroxyl dbr:Salt_(chemistry) dbr:Imidic_acid dbr:Tautomer dbr:Hydromelonate dbr:Conformational_isomer dbr:File:Heptazine_numbering.png dbr:W._Henneberg
dbp:align center (en)
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dbp:captionAlign center (en)
dbp:image Cyameluric_acid_dihydroxy_oxo_4H_form.png (en) Cyameluric_acid_hydroxy_dioxo_13H_form.png (en) Cyameluric_acid_hydroxy_dioxo_46H_form.png (en) Cyameluric_acid_trihydroxy_form.png (en) Cyameluric_acid_trioxo_134H_form.png (en) Cyameluric_acid_trioxo_136H_form.png (en) Cyameluric_acid_trioxo_form.png (en)
dbp:imagefile Cyameluric_acid_trihydroxy_form.png (en) Cyameluric_acid_trioxo_form.png (en)
dbp:iupacname 2468101213 (xsd:decimal)
dbp:name Cyameluric acid (en)
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dct:subject dbc:Heterocyclic_compounds_with_3_rings dbc:Nitrogen_heterocycles dbc:Tricyclic_compounds dbc:Triketones dbc:Lactims dbc:Amides
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rdfs:comment Cyameluric acid or 2,5,8-trihydroxy-s-heptazine is a chemical compound with formula C6N7O3H3, usually described as a heptazine molecule with the hydrogen atoms replaced by hydroxyl groups –OH; or any of its tautomers. The substance exists as an equilibrium of 17 tautomers that easily interconvert among each other. Calculations show that the symmetric tri-oxo form (1,4,7-trihydro-2,5,8-trioxo-s-heptazine) is the most stable. Therefore, this compound contains amide groups rather than imidic acids. (en)
rdfs:label Cyameluric acid (en)
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foaf:depiction wiki-commons:Special:FilePath/Heptazine_numbering.png wiki-commons:Special:FilePath/Cyameluric_acid_dihydroxy_oxo_4H_form.png wiki-commons:Special:FilePath/Cyameluric_acid_hydroxy_dioxo_13H_form.png wiki-commons:Special:FilePath/Cyameluric_acid_hydroxy_dioxo_46H_form.png wiki-commons:Special:FilePath/Cyameluric_acid_trihydroxy_form.png wiki-commons:Special:FilePath/Cyameluric_acid_trioxo_134H_form.png wiki-commons:Special:FilePath/Cyameluric_acid_trioxo_136H_form.png wiki-commons:Special:FilePath/Cyameluric_acid_trioxo_form.png
foaf:isPrimaryTopicOf wikipedia-en:Cyameluric_acid
foaf:name Cyameluric acid (en)
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