1.0 2010-04-08 22:13:41 UTC 2018-05-29 01:36:25 UTC FDB018391 Homovanillyl alcohol Isolated from various plant subspecies Constituent of mandibular secretion of honeybees [CCD] (4-Hydroxy-3-methoxyphenyl)ethanol 2-(4-Guaiacyl)-ethanol 2-(4-Hydroxy-3-methoxyphenyl)-ethanol 3-Methoxy-4-hydroxyphenylethanol 4-(2-Hydroxyethyl)-2-methoxyphenol 4-(2-Hydroxyethyl)guaiacol 4-Hydroxy-3-methoxy-benzeneethanol 4-Hydroxy-3-methoxybenzeneethanol 4-Hydroxy-3-methoxyphenethanol 4-Hydroxy-3-methoxyphenethyl alcohol 4-Hydroxy-3-methoxyphenylethyl alcohol Guaiacyl ethanol Homovanilline alcohol Homovanillyl alcohol C9H12O3 168.1898 168.07864425 4-(2-hydroxyethyl)-2-methoxyphenol homovanillyl alcohol 2380-78-1 COC1=C(O)C=CC(CCO)=C1 InChI=1S/C9H12O3/c1-12-9-6-7(4-5-10)2-3-8(9)11/h2-3,6,10-11H,4-5H2,1H3 XHUBSJRBOQIZNI-UHFFFAOYSA-N belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. Methoxyphenols Organic compounds Benzenoids Phenols Methoxyphenols Aromatic homomonocyclic compounds 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Anisoles Hydrocarbon derivatives Methoxybenzenes Phenoxy compounds Primary alcohols Tyrosols 1-hydroxy-2-unsubstituted benzenoid Alcohol Alkyl aryl ether Anisole Aromatic homomonocyclic compound Ether Hydrocarbon derivative Methoxybenzene Methoxyphenol Monocyclic benzene moiety Organic oxygen compound Organooxygen compound Phenol ether Phenoxy compound Primary alcohol Tyrosol Tyrosol derivative logp 0.95 ALOGPS logs -1.16 ALOGPS solubility 1.16e+01 g/l ALOGPS melting_point 40-42 oC logp 1.03 ChemAxon pka_strongest_acidic 10.19 ChemAxon pka_strongest_basic -2.4 ChemAxon iupac 4-(2-hydroxyethyl)-2-methoxyphenol ChemAxon average_mass 168.1898 ChemAxon mono_mass 168.07864425 ChemAxon smiles COC1=C(O)C=CC(CCO)=C1 ChemAxon formula C9H12O3 ChemAxon inchi InChI=1S/C9H12O3/c1-12-9-6-7(4-5-10)2-3-8(9)11/h2-3,6,10-11H,4-5H2,1H3 ChemAxon inchikey XHUBSJRBOQIZNI-UHFFFAOYSA-N ChemAxon polar_surface_area 49.69 ChemAxon refractivity 46.07 ChemAxon polarizability 17.67 ChemAxon rotatable_bond_count 3 ChemAxon acceptor_count 3 ChemAxon donor_count 2 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 3337 Specdb::CMs 46151 Specdb::CMs 171103 Specdb::MsMs 89064 Specdb::MsMs 89065 Specdb::MsMs 89066 Specdb::MsMs 151914 Specdb::MsMs 151915 Specdb::MsMs 151916 Specdb::MsMs 2326095 Specdb::MsMs 2326096 Specdb::MsMs 2326097 Specdb::MsMs 2612644 Specdb::MsMs 2612645 Specdb::MsMs 2612646 Specdb::MsIr 8061 Specdb::MsIr 8062 Specdb::MsIr 8063 Specdb::NmrOneD 30082 Specdb::NmrOneD 30083 Specdb::NmrOneD 30084 Specdb::NmrOneD 30085 Specdb::NmrOneD 30086 Specdb::NmrOneD 30087 Specdb::NmrOneD 30088 Specdb::NmrOneD 30089 Specdb::NmrOneD 30090 Specdb::NmrOneD 30091 Specdb::NmrOneD 30092 Specdb::NmrOneD 30093 Specdb::NmrOneD 30094 Specdb::NmrOneD 30095 Specdb::NmrOneD 30096 Specdb::NmrOneD 30097 Specdb::NmrOneD 30098 Specdb::NmrOneD 30099 Specdb::NmrOneD 30100 Specdb::NmrOneD 30101 HMDB38925 #<Reference:0x000055ce31c356b8> Olive Type 1 specific Olea europaea 4146 Olive oil Type 2