83705 1 2 3 16 16 14 1 2 3 3 2 2 1 5 255 1 2 3 3.732 2 2.866 0.5 -0.5 0 0 Compound Canonicalized 5 2021.10.14 1 Compound Complexity 7 E_COMPLEXITY 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 18.3 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 0 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 00000371000000086000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000 IUPAC Name Allowed 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 dithioxosilane IUPAC Name CAS-like Style 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 bis(sulfanylidene)silane IUPAC Name Markup 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 bis(sulfanylidene)silane IUPAC Name Preferred 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 bis(sulfanylidene)silane IUPAC Name Systematic 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 bis(sulfanylidene)silane IUPAC Name Traditional 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 dithioxosilane InChI Standard 1 1.0.6 InChI iupac.org 2021.10.14 InChI=1S/S2Si/c1-3-2 InChIKey Standard 1 1.0.6 InChI iupac.org 2021.10.14 KHDSWONFYIAAPE-UHFFFAOYSA-N Mass Exact 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 91.92106888 Molecular Formula 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 S2Si Molecular Weight 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 92.22 SMILES Canonical 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 [Si](=S)=S SMILES Isomeric 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 [Si](=S)=S Topological Polar Surface Area 7 E_TPSA 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 64.2 Weight MonoIsotopic 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 91.92106888 3 0 0 0 0 0 0 0 1 -1