16682746 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 50 50 8 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 2 2 2 2 4 4 4 5 5 5 6 6 6 7 7 7 8 8 8 9 9 9 10 10 10 11 11 11 12 12 12 13 13 13 14 14 14 15 15 15 16 16 16 17 17 17 18 18 18 19 19 19 20 20 20 21 21 21 22 22 22 23 23 23 24 24 24 25 25 25 26 26 26 27 27 27 3 4 5 6 3 7 8 9 10 28 29 11 30 31 12 32 33 13 34 35 14 36 37 15 38 39 16 40 41 17 42 43 18 44 45 19 46 47 20 48 49 21 50 51 22 52 53 23 54 55 24 56 57 25 58 59 26 60 61 27 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 5 255 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 5.4641 7.1962 6.3301 4.5981 4.9641 5.9641 8.0622 7.6962 6.6962 3.732 5.4641 5.4641 8.9282 7.1962 7.1962 2.866 4.9641 5.9641 9.7942 7.6962 8.1962 2 5.4641 5.4641 10.6603 8.6962 8.6962 4.1996 4.9966 4.4892 4.4892 6.439 6.439 7.6636 8.4607 8.1711 8.1711 6.2212 6.2212 4.1306 3.3335 5.939 5.939 4.9892 4.9892 9.3267 8.5297 6.7212 6.7212 6.6135 7.3038 2.4675 3.2646 4.4892 4.4892 6.439 6.439 9.3957 10.1928 7.8038 7.1135 8.7788 8.0885 2.31 1.4631 1.69 6.001 5.7741 4.9272 4.9272 5.1541 6.001 10.9703 11.1972 10.3503 8.6962 9.3162 8.6962 8.1592 9.0062 9.2331 0 0 0.5 -0.5 0.866 -0.866 -0.5 0.866 -0.866 -0 1.732 -1.732 -0 1.732 -1.732 -0.5 2.5981 -2.5981 -0.5 2.5981 -1.732 -0 3.4641 -3.4641 -0 2.5981 -2.5981 -0.9749 -0.9749 1.2646 0.4675 -1.2646 -0.4675 -0.9749 -0.9749 0.4675 1.2646 -0.4675 -1.2646 0.4749 0.4749 1.3335 2.1306 -1.3335 -2.1306 0.4749 0.4749 2.1306 1.3335 -1.9441 -2.3426 -0.9749 -0.9749 2.9966 2.1996 -2.9966 -2.1996 -0.9749 -0.9749 3.2087 2.8101 -1.52 -1.1215 0.5369 0.31 -0.5369 3.1541 4.001 3.7741 -3.1541 -4.001 -3.7741 -0.5369 0.31 0.5369 1.9781 2.5981 3.2181 -2.9081 -3.135 -2.2881 0 Compound Canonicalized 5 2021.10.14 1 Compound Complexity 7 E_COMPLEXITY 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 246 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 1 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 20 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 00000371F07820000000000000008000000000000000000000000000000000000000000000000018000000000008008000000200000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000 IUPAC Name Allowed 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 tributyl(tributylstannyloxy)stannane IUPAC Name CAS-like Style 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 tributyl(tributylstannyloxy)stannane IUPAC Name Markup 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 tributyl(tributylstannyloxy)stannane IUPAC Name Preferred 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 tributyl(tributylstannyloxy)stannane IUPAC Name Systematic 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 tributyl(tributylstannyloxy)stannane IUPAC Name Traditional 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 tributyl(tributylstannyloxy)stannane InChI Standard 1 1.0.6 InChI iupac.org 2021.10.14 InChI=1S/6C4H9.O.2Sn/c6*1-3-4-2;;;/h6*1,3-4H2,2H3;;; InChIKey Standard 1 1.0.6 InChI iupac.org 2021.10.14 APQHKWPGGHMYKJ-UHFFFAOYSA-N Mass Exact 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 596.22128 Molecular Formula 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 C24H54OSn2 Molecular Weight 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 596.1 SMILES Canonical 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC SMILES Isomeric 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC Topological Polar Surface Area 7 E_TPSA 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 9.2 Weight MonoIsotopic 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 598.22187 27 0 0 0 0 0 0 0 1 -1