1.0 2010-04-08 22:13:51 UTC 2025-11-19 02:13:06 UTC FDB018653 Torachrysone 8-(6-oxalylglucoside) Constituent of a Rhei species Torachrysone 8-(6-oxalylglucoside) is found in green vegetables. Torachrysone 8-(6-oxalylglucoside) C22H24O12 480.4188 480.126776232 {6-[(7-acetyl-8-hydroxy-3-methoxy-6-methylnaphthalen-1-yl)oxy]-3,4,5-trihydroxyoxan-2-yl}methyl hydrogen oxalate {6-[(7-acetyl-8-hydroxy-3-methoxy-6-methylnaphthalen-1-yl)oxy]-3,4,5-trihydroxyoxan-2-yl}methyl hydrogen oxalate 64078-76-8 COC1=CC(OC2OC(COC(=O)C(O)=O)C(O)C(O)C2O)=C2C(O)=C(C(C)=O)C(C)=CC2=C1 InChI=1S/C22H24O12/c1-8-4-10-5-11(31-3)6-12(15(10)17(25)14(8)9(2)23)33-22-19(27)18(26)16(24)13(34-22)7-32-21(30)20(28)29/h4-6,13,16,18-19,22,24-27H,7H2,1-3H3,(H,28,29) DVKQFBNYDILOTK-UHFFFAOYSA-N belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. Phenolic glycosides Organic compounds Organic oxygen compounds Organooxygen compounds Carbohydrates and carbohydrate conjugates Aromatic heteropolycyclic compounds 1-hydroxy-4-unsubstituted benzenoids Acetals Acetophenones Alkyl aryl ethers Anisoles Aryl alkyl ketones Carboxylic acid esters Carboxylic acids Dicarboxylic acids and derivatives Hydrocarbon derivatives Monosaccharides Naphthols and derivatives O-glycosyl compounds Organic oxides Oxacyclic compounds Oxanes Polyols Secondary alcohols Vinylogous acids 1-hydroxy-4-unsubstituted benzenoid 1-naphthol Acetal Acetophenone Alcohol Alkyl aryl ether Anisole Aromatic heteropolycyclic compound Aryl alkyl ketone Aryl ketone Benzenoid Carbonyl group Carboxylic acid Carboxylic acid derivative Carboxylic acid ester Dicarboxylic acid or derivatives Ether Hydrocarbon derivative Ketone Monosaccharide Naphthalene O-glycosyl compound Organic oxide Organoheterocyclic compound Oxacycle Oxane Phenolic glycoside Polyol Secondary alcohol Vinylogous acid logp 0.73 ALOGPS logs -2.73 ALOGPS solubility 8.87e-01 g/l ALOGPS logp 1.28 ChemAxon pka_strongest_acidic 1.94 ChemAxon pka_strongest_basic -3.6 ChemAxon iupac {6-[(7-acetyl-8-hydroxy-3-methoxy-6-methylnaphthalen-1-yl)oxy]-3,4,5-trihydroxyoxan-2-yl}methyl hydrogen oxalate ChemAxon average_mass 480.4188 ChemAxon mono_mass 480.126776232 ChemAxon smiles COC1=CC(OC2OC(COC(=O)C(O)=O)C(O)C(O)C2O)=C2C(O)=C(C(C)=O)C(C)=CC2=C1 ChemAxon formula C22H24O12 ChemAxon inchi InChI=1S/C22H24O12/c1-8-4-10-5-11(31-3)6-12(15(10)17(25)14(8)9(2)23)33-22-19(27)18(26)16(24)13(34-22)7-32-21(30)20(28)29/h4-6,13,16,18-19,22,24-27H,7H2,1-3H3,(H,28,29) ChemAxon inchikey DVKQFBNYDILOTK-UHFFFAOYSA-N ChemAxon polar_surface_area 189.28 ChemAxon refractivity 111.47 ChemAxon polarizability 46.27 ChemAxon rotatable_bond_count 8 ChemAxon acceptor_count 11 ChemAxon donor_count 5 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 14153 Specdb::CMs 46278 Specdb::CMs 134428 Specdb::CMs 142162 Specdb::MsMs 88335 Specdb::MsMs 88336 Specdb::MsMs 88337 Specdb::MsMs 151032 Specdb::MsMs 151033 Specdb::MsMs 151034 Specdb::MsMs 2743726 Specdb::MsMs 2743727 Specdb::MsMs 2743728 Specdb::MsMs 2934432 Specdb::MsMs 2934433 Specdb::MsMs 2934434 HMDB39135 #<Reference:0x000055ce3246de48> Green vegetables Unknown generic