{"ymdb_id":"YMDB16085","created_at":"2016-08-03T23:52:58.000Z","updated_at":"2016-09-11T18:51:04.000Z","name":"Tetrahydronaphthalene","cas":null,"state":null,"melting_point":null,"description":"Tetrahydronaphthalene belongs to the class of chemical entities known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane.","experimental_water_solubility":null,"experimental_logp_hydrophobicity":null,"location":null,"synthesis_reference":null,"chebi_id":null,"hmdb_id":null,"kegg_id":null,"pubchem_id":null,"cs_id":null,"foodb_id":null,"wikipedia_link":null,"biocyc_id":null,"iupac":"1,2,3,4-tetrahydronaphthalene","traditional_iupac":"tetralin","logp":"3.4255000219999996","pka":null,"alogps_solubility":"2.46e-02 g/l","alogps_logp":"3.79","alogps_logs":"-3.73","acceptor_count":"0","donor_count":"0","rotatable_bond_count":"0","polar_surface_area":"0.0","refractivity":"43.5402","polarizability":"16.032306224573407","formal_charge":"0","physiological_charge":"0","pka_strongest_basic":null,"pka_strongest_acidic":null,"bioavailability":"1","number_of_rings":"2","rule_of_five":"1","ghose_filter":"0","veber_rule":"1","mddr_like_rule":"0","synonyms":[],"pathways":[],"growth_conditions":[],"references":[{"pubmed_id":19845354,"citation":"Robinson AL, Ebeler SE, Heymann H, Boss PK, Solomon PS, Trengove RD. (2009). \"Interactions between wine volatile compounds and grape and wine matrix components influence aroma compound headspace partitioning.\" J Agric Food Chem. 2009 Nov 11;57(21):10313-22."}],"proteins":[]}