1.0 2010-04-08 22:10:51 UTC 2025-11-19 00:28:41 UTC FDB013679 1-(3-Hydroxy-4-Methoxyphenyl)-1,2-ethanediol 3'-O-b-D-glucoside Constituent of fennel (Foeniculum vulgare). 1-(3-Hydroxy-4-Methoxyphenyl)-1,2-ethanediol 3'-O-b-D-glucoside is found in herbs and spices. 1-(3-Hydroxy-4-Methoxyphenyl)-1,2-ethanediol 3'-O-b-D-glucopyranoside C15H22O9 346.3298 346.126382302 2-[5-(1,2-dihydroxyethyl)-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 2-[5-(1,2-dihydroxyethyl)-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 217972-13-9 COC1=C(OC2OC(CO)C(O)C(O)C2O)C=C(C=C1)C(O)CO InChI=1S/C15H22O9/c1-22-9-3-2-7(8(18)5-16)4-10(9)23-15-14(21)13(20)12(19)11(6-17)24-15/h2-4,8,11-21H,5-6H2,1H3 CEAVUNYMFVXZKB-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 Alkyl aryl ethers Anisoles Aromatic alcohols Hexoses Hydrocarbon derivatives Methoxybenzenes O-glycosyl compounds Oxacyclic compounds Oxanes Phenoxy compounds Polyols Primary alcohols Secondary alcohols Acetal Alcohol Alkyl aryl ether Anisole Aromatic alcohol Aromatic heteromonocyclic compound Benzenoid Ether Hexose monosaccharide Hydrocarbon derivative Methoxybenzene Monocyclic benzene moiety Monosaccharide O-glycosyl compound Organoheterocyclic compound Oxacycle Oxane Phenol ether Phenolic glycoside Phenoxy compound Polyol Primary alcohol Secondary alcohol logp -1.32 ALOGPS logs -1.39 ALOGPS solubility 1.42e+01 g/l ALOGPS logp -2.2 ChemAxon pka_strongest_acidic 12.18 ChemAxon pka_strongest_basic -3 ChemAxon iupac 2-[5-(1,2-dihydroxyethyl)-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol ChemAxon average_mass 346.3298 ChemAxon mono_mass 346.126382302 ChemAxon smiles COC1=C(OC2OC(CO)C(O)C(O)C2O)C=C(C=C1)C(O)CO ChemAxon formula C15H22O9 ChemAxon inchi InChI=1S/C15H22O9/c1-22-9-3-2-7(8(18)5-16)4-10(9)23-15-14(21)13(20)12(19)11(6-17)24-15/h2-4,8,11-21H,5-6H2,1H3 ChemAxon inchikey CEAVUNYMFVXZKB-UHFFFAOYSA-N ChemAxon polar_surface_area 149.07 ChemAxon refractivity 79.42 ChemAxon polarizability 33.52 ChemAxon rotatable_bond_count 6 ChemAxon acceptor_count 9 ChemAxon donor_count 6 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 91854 Specdb::MsMs 91855 Specdb::MsMs 91856 Specdb::MsMs 155343 Specdb::MsMs 155344 Specdb::MsMs 155345 Specdb::MsMs 2384987 Specdb::MsMs 2384988 Specdb::MsMs 2384989 Specdb::MsMs 2577612 Specdb::MsMs 2577613 Specdb::MsMs 2577614 Specdb::CMs 23904 Specdb::CMs 44166 Specdb::CMs 149170 Specdb::CMs 149172 Specdb::CMs 149174 Specdb::CMs 149176 Specdb::CMs 149295 Specdb::CMs 279711 Specdb::NmrOneD 129878 Specdb::NmrOneD 129879 Specdb::NmrOneD 129880 Specdb::NmrOneD 129881 Specdb::NmrOneD 129882 Specdb::NmrOneD 129883 Specdb::NmrOneD 129884 Specdb::NmrOneD 129885 Specdb::NmrOneD 129886 Specdb::NmrOneD 129887 Specdb::NmrOneD 129888 Specdb::NmrOneD 129889 Specdb::NmrOneD 129890 Specdb::NmrOneD 129891 Specdb::NmrOneD 129892 Specdb::NmrOneD 129893 Specdb::NmrOneD 129894 Specdb::NmrOneD 129895 Specdb::NmrOneD 129896 Specdb::NmrOneD 129897 HMDB35057 #<Reference:0x000055ce325011e8> Herbs and Spices Unknown generic