61600 1 2 3 4 5 6 7 82 7 7 7 7 7 7 4 1 5 1 6 -1 7 -1 1 1 2 3 4 5 2 3 4 5 6 7 1 1 2 2 2 2 2 -1 1 4 -1 6 3 1 3 -1 1 5 -1 7 3 1 1 5 255 1 2 3 4 5 6 7 4.5981 5.4641 3.732 6.3301 2.866 7.1962 2 0 0.5 0.5 0 -0 -0.5 -0.5 1 1 2 3 4 5 0 Compound Canonicalized 5 2019.01.04 1 Compound Complexity 7 E_COMPLEXITY 3.4.6.11 Cactvs xemistry.com 2019.06.18 107 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.4.6.11 Cactvs xemistry.com 2019.06.18 4 Count Hydrogen Bond Donor 5 E_NHDONORS 3.4.6.11 Cactvs xemistry.com 2019.06.18 0 Count Rotatable Bond 5 E_NROTBONDS 3.4.6.11 Cactvs xemistry.com 2019.06.18 2 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.4.6.11 Cactvs xemistry.com 2019.06.18 00000371000380000000000000000000400000000000000000000000000000000000000000000000000800000000000000000000000000000200000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000 IUPAC Name Allowed 1 2.6.6 LexiChem openeye.com 2019.06.18 diazidolead IUPAC Name CAS-like Style 1 2.6.6 LexiChem openeye.com 2019.06.18 diazidolead IUPAC Name Markup 1 2.6.6 LexiChem openeye.com 2019.06.18 diazidolead IUPAC Name Preferred 1 2.6.6 LexiChem openeye.com 2019.06.18 diazidolead IUPAC Name Systematic 1 2.6.6 LexiChem openeye.com 2019.06.18 diazidolead IUPAC Name Traditional 1 2.6.6 LexiChem openeye.com 2019.06.18 diazidolead InChI Standard 1 1.0.5 InChI iupac.org 2019.06.18 InChI=1S/2N3.Pb/c2*1-3-2;/q2*-1;+2 InChIKey Standard 1 1.0.5 InChI iupac.org 2019.06.18 ISEQAARZRCDNJH-UHFFFAOYSA-N Mass Exact 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 291.99510 Molecular Formula 1 2.1 PubChem ncbi.nlm.nih.gov 2019.06.18 N6Pb Molecular Weight 1 2.1 PubChem ncbi.nlm.nih.gov 2021.08.13 291 SMILES Canonical 1 2.1.5 OEChem openeye.com 2019.06.18 [N-]=[N+]=N[Pb]N=[N+]=[N-] SMILES Isomeric 1 2.1.5 OEChem openeye.com 2019.06.18 [N-]=[N+]=N[Pb]N=[N+]=[N-] Topological Polar Surface Area 7 E_TPSA 3.4.6.11 Cactvs xemistry.com 2019.06.18 28.7 Weight MonoIsotopic 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 291.99510 7 0 0 0 2 0 2 0 1 -1