1.0 2010-04-08 22:10:39 UTC 2025-11-18 23:43:39 UTC FDB013337 cis-p-Menthane-1,7,8-triol 8-glucoside Constituent of Foeniculum vulgare (fennel). cis-p-Menthane-1,7,8-triol 8-glucoside is found in herbs and spices. cis-p-Menthane-1,7,8-triol 8-glucoside cis-p-Menthane-1,7,8-triol 8-O-b-D-glucopyranoside C16H30O8 350.4046 350.194067936 2-({2-[4-hydroxy-4-(hydroxymethyl)cyclohexyl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol 2-({2-[4-hydroxy-4-(hydroxymethyl)cyclohexyl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol 217962-29-3 CC(C)(OC1OC(CO)C(O)C(O)C1O)C1CCC(O)(CO)CC1 InChI=1S/C16H30O8/c1-15(2,9-3-5-16(22,8-18)6-4-9)24-14-13(21)12(20)11(19)10(7-17)23-14/h9-14,17-22H,3-8H2,1-2H3 PHDIOUHOXBJRFB-UHFFFAOYSA-N belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. O-glycosyl compounds Organic compounds Organic oxygen compounds Organooxygen compounds Carbohydrates and carbohydrate conjugates Aliphatic heteromonocyclic compounds Acetals Cyclic alcohols and derivatives Cyclohexanols Hexoses Hydrocarbon derivatives Menthane monoterpenoids Monocyclic monoterpenoids Oxacyclic compounds Oxanes Polyols Primary alcohols Tertiary alcohols Acetal Alcohol Aliphatic heteromonocyclic compound Cyclic alcohol Cyclohexanol Hexose monosaccharide Hydrocarbon derivative Monocyclic monoterpenoid Monosaccharide Monoterpenoid O-glycosyl compound Organoheterocyclic compound Oxacycle Oxane P-menthane monoterpenoid Polyol Primary alcohol Secondary alcohol Tertiary alcohol logp -1.23 ALOGPS logs -1.19 ALOGPS solubility 2.29e+01 g/l ALOGPS logp -1.6 ChemAxon pka_strongest_acidic 12.2 ChemAxon pka_strongest_basic -3 ChemAxon iupac 2-({2-[4-hydroxy-4-(hydroxymethyl)cyclohexyl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol ChemAxon average_mass 350.4046 ChemAxon mono_mass 350.194067936 ChemAxon smiles CC(C)(OC1OC(CO)C(O)C(O)C1O)C1CCC(O)(CO)CC1 ChemAxon formula C16H30O8 ChemAxon inchi InChI=1S/C16H30O8/c1-15(2,9-3-5-16(22,8-18)6-4-9)24-14-13(21)12(20)11(19)10(7-17)23-14/h9-14,17-22H,3-8H2,1-2H3 ChemAxon inchikey PHDIOUHOXBJRFB-UHFFFAOYSA-N ChemAxon polar_surface_area 139.84 ChemAxon refractivity 83.33 ChemAxon polarizability 36.42 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 8 ChemAxon donor_count 6 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 18558 Specdb::CMs 44047 Specdb::CMs 153875 Specdb::MsMs 55152 Specdb::MsMs 55153 Specdb::MsMs 55154 Specdb::MsMs 114273 Specdb::MsMs 114274 Specdb::MsMs 114275 Specdb::MsMs 2827011 Specdb::MsMs 2827012 Specdb::MsMs 2827013 Specdb::MsMs 2851423 Specdb::MsMs 2851424 Specdb::MsMs 2851425 Specdb::NmrOneD 127778 Specdb::NmrOneD 127779 Specdb::NmrOneD 127780 Specdb::NmrOneD 127781 Specdb::NmrOneD 127782 Specdb::NmrOneD 127783 Specdb::NmrOneD 127784 Specdb::NmrOneD 127785 Specdb::NmrOneD 127786 Specdb::NmrOneD 127787 Specdb::NmrOneD 127788 Specdb::NmrOneD 127789 Specdb::NmrOneD 127790 Specdb::NmrOneD 127791 Specdb::NmrOneD 127792 Specdb::NmrOneD 127793 Specdb::NmrOneD 127794 Specdb::NmrOneD 127795 Specdb::NmrOneD 127796 Specdb::NmrOneD 127797 HMDB0034784 Herbs and Spices Unknown generic