1.0 2010-04-08 22:15:43 UTC 2018-05-29 01:51:30 UTC FDB021481 Dihydroconiferin Constituent of Pinus sylvestris (Scotch pine) 5,6-disubstituted anthranilic acid sulfonamide, 9a Dihydroconiferin C16H24O8 344.357 344.147117744 2-(hydroxymethyl)-6-[4-(3-hydroxypropyl)-2-methoxyphenoxy]oxane-3,4,5-triol 2-(hydroxymethyl)-6-[4-(3-hydroxypropyl)-2-methoxyphenoxy]oxane-3,4,5-triol 17609-06-2 COC1=C(OC2OC(CO)C(O)C(O)C2O)C=CC(CCCO)=C1 InChI=1S/C16H24O8/c1-22-11-7-9(3-2-6-17)4-5-10(11)23-16-15(21)14(20)13(19)12(8-18)24-16/h4-5,7,12-21H,2-3,6,8H2,1H3 QFYFLJZBZITPGX-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 Hydrocarbon derivatives Methoxybenzenes Monosaccharides O-glycosyl compounds Oxacyclic compounds Oxanes Phenoxy compounds Polyols Primary alcohols Secondary alcohols Acetal Alcohol Alkyl aryl ether Anisole Aromatic heteromonocyclic compound Benzenoid Ether 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 a small molecule logp -0.36 ALOGPS logs -1.81 ALOGPS solubility 5.29e+00 g/l ALOGPS melting_point Mp 143° (130-132°) logp -0.79 ChemAxon pka_strongest_acidic 12.2 ChemAxon pka_strongest_basic -2.4 ChemAxon iupac 2-(hydroxymethyl)-6-[4-(3-hydroxypropyl)-2-methoxyphenoxy]oxane-3,4,5-triol ChemAxon average_mass 344.357 ChemAxon mono_mass 344.147117744 ChemAxon smiles COC1=C(OC2OC(CO)C(O)C(O)C2O)C=CC(CCCO)=C1 ChemAxon formula C16H24O8 ChemAxon inchi InChI=1S/C16H24O8/c1-22-11-7-9(3-2-6-17)4-5-10(11)23-16-15(21)14(20)13(19)12(8-18)24-16/h4-5,7,12-21H,2-3,6,8H2,1H3 ChemAxon inchikey QFYFLJZBZITPGX-UHFFFAOYSA-N ChemAxon polar_surface_area 128.84 ChemAxon refractivity 82.82 ChemAxon polarizability 35.28 ChemAxon rotatable_bond_count 7 ChemAxon acceptor_count 8 ChemAxon donor_count 5 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 14861 Specdb::CMs 47355 Specdb::CMs 170713 Specdb::NmrOneD 47122 Specdb::NmrOneD 47123 Specdb::NmrOneD 47124 Specdb::NmrOneD 47125 Specdb::NmrOneD 47126 Specdb::NmrOneD 47127 Specdb::NmrOneD 47128 Specdb::NmrOneD 47129 Specdb::NmrOneD 47130 Specdb::NmrOneD 47131 Specdb::NmrOneD 47132 Specdb::NmrOneD 47133 Specdb::NmrOneD 47134 Specdb::NmrOneD 47135 Specdb::NmrOneD 47136 Specdb::NmrOneD 47137 Specdb::NmrOneD 47138 Specdb::NmrOneD 47139 Specdb::NmrOneD 47140 Specdb::NmrOneD 47141 Specdb::MsMs 298840 Specdb::MsMs 298841 Specdb::MsMs 298842 Specdb::MsMs 340717 Specdb::MsMs 340718 Specdb::MsMs 340719 Specdb::MsMs 2333983 Specdb::MsMs 2333984 Specdb::MsMs 2333985 Specdb::MsMs 2632484 Specdb::MsMs 2632485 Specdb::MsMs 2632486 HMDB41509 #<Reference:0x000055ce3264e9b0>