157350 1 2 8 1 1 2 1 2 1 1 5 255 1 2 3 2 0 0 0 Compound Canonicalized 5 2019.01.04 1 Compound Complexity 7 E_COMPLEXITY 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 0 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 0 Count Hydrogen Bond Donor 5 E_NHDONORS 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 1 Count Rotatable Bond 5 E_NROTBONDS 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 0 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 00000371000020000000000000000000000000000000000000000000000000000000000000000000000008000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000 IUPAC Name Allowed 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 lambda1-oxidane IUPAC Name CAS-like Style 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 lambda1-oxidane IUPAC Name Markup 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 &lambda;<SUP>1</SUP>-oxidane IUPAC Name Preferred 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 lambda1-oxidane IUPAC Name Systematic 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 lambda1-oxidane IUPAC Name Traditional 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 lambda1-oxidane InChI Standard 1 1.0.6 InChI iupac.org 2021.05.07 InChI=1S/HO/h1H InChIKey Standard 1 1.0.6 InChI iupac.org 2021.05.07 TUJKJAMUKRIRHC-UHFFFAOYSA-N Log P XLogP3-AA 7 3.0 sioc-ccbg.ac.cn 2021.05.07 -0.5 Mass Exact 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 17.002739651 Molecular Formula 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 HO Molecular Weight 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 17.007 SMILES Canonical 1 2.3.0 OEChem OpenEye Scientific Software 2021.05.07 [OH] SMILES Isomeric 1 2.3.0 OEChem OpenEye Scientific Software 2021.05.07 [OH] Topological Polar Surface Area 7 E_TPSA 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 1 Weight MonoIsotopic 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 17.002739651 1 0 0 0 0 0 0 0 1 -1