123195 1 2 3 4 7 7 1 1 1 1 2 2 3 4 2 1 1 1 5 255 1 2 3 4 2.5369 3.403 2 3.9399 -0.25 0.25 0.06 -0.06 0 Compound Canonicalized 5 2021.10.14 1 Compound Complexity 7 E_COMPLEXITY 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 0 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 2 Count Hydrogen Bond Donor 5 E_NHDONORS 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 2 Count Rotatable Bond 5 E_NROTBONDS 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 0 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 00000371000300000000000000000000000000000000000000000000000000000000000000000000001800000000000000000000000200000200000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000 IUPAC Name Allowed 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 diazene IUPAC Name CAS-like Style 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 diazene IUPAC Name Markup 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 diazene IUPAC Name Preferred 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 diazene IUPAC Name Systematic 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 diazene IUPAC Name Traditional 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 diazene InChI Standard 1 1.0.6 InChI iupac.org 2021.10.14 InChI=1S/H2N2/c1-2/h1-2H InChIKey Standard 1 1.0.6 InChI iupac.org 2021.10.14 RAABOESOVLLHRU-UHFFFAOYSA-N Log P XLogP3-AA 7 3.0 sioc-ccbg.ac.cn 2021.10.14 1.5 Mass Exact 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 30.021798072 Molecular Formula 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 H2N2 Molecular Weight 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 30.030 SMILES Canonical 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 N=N SMILES Isomeric 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 N=N Topological Polar Surface Area 7 E_TPSA 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 47.7 Weight MonoIsotopic 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 30.021798072 2 0 0 0 0 0 0 0 1 -1