1.0 2010-04-08 22:13:14 UTC 2019-11-26 03:15:01 UTC FDB017669 Dihydromelilotoside Isolated from Chinese cinnamon. Dihydromelilotoside is found in herbs and spices. Cryptamygin B Dihydromelilotoside C15H20O8 328.3145 328.115817616 3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)propanoic acid 3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)propanoic acid 24696-05-7 OCC1OC(OC2=CC=CC=C2CCC(O)=O)C(O)C(O)C1O InChI=1S/C15H20O8/c16-7-10-12(19)13(20)14(21)15(23-10)22-9-4-2-1-3-8(9)5-6-11(17)18/h1-4,10,12-16,19-21H,5-7H2,(H,17,18) FXEOLMWSBWXMSF-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 heteromonocyclic compounds Acetals Carbonyl compounds Carboxylic acids Hexoses Hydrocarbon derivatives Monocarboxylic acids and derivatives O-glycosyl compounds Organic oxides Oxacyclic compounds Oxanes Phenol ethers Phenoxy compounds Phenylpropanoic acids Polyols Primary alcohols Secondary alcohols 3-phenylpropanoic-acid Acetal Alcohol Aromatic heteromonocyclic compound Benzenoid Carbonyl group Carboxylic acid Carboxylic acid derivative Hexose monosaccharide Hydrocarbon derivative Monocarboxylic acid or derivatives Monocyclic benzene moiety Monosaccharide O-glycosyl compound Organic oxide Organoheterocyclic compound Oxacycle Oxane Phenol ether Phenolic glycoside Phenoxy compound Polyol Primary alcohol Secondary alcohol logp -0.43 ALOGPS logs -1.68 ALOGPS solubility 6.82e+00 g/l ALOGPS melting_point Mp 144-145° logp -0.52 ChemAxon pka_strongest_acidic 3.83 ChemAxon pka_strongest_basic -3 ChemAxon iupac 3-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)propanoic acid ChemAxon average_mass 328.3145 ChemAxon mono_mass 328.115817616 ChemAxon smiles OCC1OC(OC2=CC=CC=C2CCC(O)=O)C(O)C(O)C1O ChemAxon formula C15H20O8 ChemAxon inchi InChI=1S/C15H20O8/c16-7-10-12(19)13(20)14(21)15(23-10)22-9-4-2-1-3-8(9)5-6-11(17)18/h1-4,10,12-16,19-21H,5-7H2,(H,17,18) ChemAxon inchikey FXEOLMWSBWXMSF-UHFFFAOYSA-N ChemAxon polar_surface_area 136.68 ChemAxon refractivity 76.09 ChemAxon polarizability 31.98 ChemAxon rotatable_bond_count 6 ChemAxon acceptor_count 8 ChemAxon donor_count 5 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::NmrOneD 25822 Specdb::NmrOneD 25823 Specdb::NmrOneD 25824 Specdb::NmrOneD 25825 Specdb::NmrOneD 25826 Specdb::NmrOneD 25827 Specdb::NmrOneD 25828 Specdb::NmrOneD 25829 Specdb::NmrOneD 25830 Specdb::NmrOneD 25831 Specdb::NmrOneD 25832 Specdb::NmrOneD 25833 Specdb::NmrOneD 25834 Specdb::NmrOneD 25835 Specdb::NmrOneD 25836 Specdb::NmrOneD 25837 Specdb::NmrOneD 25838 Specdb::NmrOneD 25839 Specdb::NmrOneD 25840 Specdb::NmrOneD 25841 Specdb::CMs 13350 Specdb::CMs 45768 Specdb::CMs 170428 Specdb::MsMs 43032 Specdb::MsMs 43033 Specdb::MsMs 43034 Specdb::MsMs 158172 Specdb::MsMs 158173 Specdb::MsMs 158174 Specdb::MsMs 2247441 Specdb::MsMs 2302335 Specdb::MsMs 2302336 Specdb::MsMs 2302337 Specdb::MsMs 3066353 Specdb::MsMs 3066354 Specdb::MsMs 3066355 HMDB38334 #<Reference:0x000055ce31a16a30> Herbs and Spices Unknown generic