Mrv1652309272007342D 11 11 0 0 0 0 999 V2000 9980.8636 9979.0116 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9980.1527 9978.6010 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9979.4383 9979.0135 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9978.7236 9978.6008 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9978.7236 9977.7758 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9979.4381 9977.3633 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9980.1527 9977.7758 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9978.0107 9977.3643 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9981.5766 9978.6001 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9979.4380 9976.5401 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9980.1508 9976.1284 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2 3 2 0 0 0 0 3 4 1 0 0 0 0 4 5 2 0 0 0 0 5 6 1 0 0 0 0 6 7 2 0 0 0 0 7 2 1 0 0 0 0 2 1 1 0 0 0 0 5 8 1 0 0 0 0 1 9 2 0 0 0 0 6 10 1 0 0 0 0 10 11 1 0 0 0 0 M END > <DATABASE_ID> CDB005772 > <DATABASE_NAME> CDB > <SMILES> COC1=CC(C=O)=CC=C1O > <INCHI_IDENTIFIER> InChI=1S/C8H8O3/c1-11-8-4-6(5-9)2-3-7(8)10/h2-5,10H,1H3 > <INCHI_KEY> MWOOGOJBHIARFG-UHFFFAOYSA-N > <FORMULA> C8H8O3 > <MOLECULAR_WEIGHT> 152.1473 > <EXACT_MASS> 152.047344122 > <JCHEM_ACCEPTOR_COUNT> 3 > <JCHEM_ATOM_COUNT> 19 > <JCHEM_AVERAGE_POLARIZABILITY> 14.81738516647897 > <JCHEM_BIOAVAILABILITY> 1 > <JCHEM_DONOR_COUNT> 1 > <JCHEM_FORMAL_CHARGE> 0 > <JCHEM_GHOSE_FILTER> 0 > <JCHEM_IUPAC> 4-hydroxy-3-methoxybenzaldehyde > <ALOGPS_LOGP> 1.31 > <JCHEM_LOGP> 1.224511573333333 > <ALOGPS_LOGS> -1.48 > <JCHEM_MDDR_LIKE_RULE> 0 > <JCHEM_NUMBER_OF_RINGS> 1 > <JCHEM_PHYSIOLOGICAL_CHARGE> 0 > <JCHEM_PKA_STRONGEST_ACIDIC> 7.807246236597697 > <JCHEM_PKA_STRONGEST_BASIC> -4.895506955382694 > <JCHEM_POLAR_SURFACE_AREA> 46.53 > <JCHEM_REFRACTIVITY> 41.0861 > <JCHEM_ROTATABLE_BOND_COUNT> 2 > <JCHEM_RULE_OF_FIVE> 1 > <ALOGPS_SOLUBILITY> 5.05e+00 g/l > <JCHEM_TRADITIONAL_IUPAC> vanillin > <JCHEM_VEBER_RULE> 0 > <Cannabis Database ID> CDB005772 > <GENERIC_NAME> Vanillin $$$$