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2 2 2 2 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 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 131 132 133 134 135 136 137 16.278 15.0955 14.2799 14.6627 20.4603 21.2965 19.6241 19.7693 24.6426 26.0909 26.0909 25.7477 14.6899 14.2568 13.0744 12.8693 20.3163 18.789 18.6439 19.4801 16.7511 18.4235 17.5875 18.0369 0.866 4.5981 8.3301 21.3263 19.4801 0.866 4.5981 8.3301 19.4801 0.866 19.4801 13.5955 17.9511 22.9695 19.4801 18.9031 16.363 15.8848 8.3301 16.9708 12.2087 19.648 17.9229 11.1962 20.3461 27.764 25.7479 21.9893 27.5909 20.3461 20.3461 18.614 1.732 0 5.4641 3.732 9.1962 7.4641 1.732 0 20.3461 18.614 9.1962 7.4641 20.3461 18.614 18.614 16.0281 15.2896 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27.8063 27.8063 3 11.9385 13.3218 13.5539 12.053 12.4179 13.9873 12.9401 12.9401 12.5848 11.6718 11.0627 11.4918 10.3978 11.9143 9.9775 9.4054 11.0781 10.8429 8.2922 9.475 9.1211 7.9869 7.4045 9.0428 18.946 19.5552 20.8235 19.3752 20.4681 20.8235 6.5168 7.9652 8.0172 7.875 7.9936 9.4139 13.13 10.8226 15.9229 14.17 14.4229 11.2675 12.6817 10.5395 10.8192 10.5007 12.7803 9.0716 9.9318 5 9.7923 7.6752 19.1508 18.4228 20.565 22.3063 6.4998 6.7404 8.7069 9.0396 11.9031 10.9031 13.1531 12.1531 11.9031 10.9031 0 Compound Canonicalized 5 2021.10.14 1 Compound Complexity 7 E_COMPLEXITY 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 207 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 84 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 0000037100003FFC0000200000000000000000000000000000002448912240000000000000000000000000400000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000000 IUPAC Name Allowed 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 hexadecamagnesium;decasodium;dioxosilane;1,3,5,7-tetraoxido-2,4,6,8,9,10-hexaoxa-1,3,5,7-tetrasilatricyclo[3.3.1.13,7]decane;octadecafluoride IUPAC Name CAS-like Style 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 hexadecamagnesium;decasodium;dioxosilane;1,3,5,7-tetraoxido-2,4,6,8,9,10-hexaoxa-1,3,5,7-tetrasilatricyclo[3.3.1.13,7]decane;octadecafluoride IUPAC Name Markup 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 hexadecamagnesium;decasodium;dioxosilane;1,3,5,7-tetraoxido-2,4,6,8,9,10-hexaoxa-1,3,5,7-tetrasilatricyclo[3.3.1.1<SUP>3,7</SUP>]decane;octadecafluoride IUPAC Name Preferred 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 hexadecamagnesium;decasodium;dioxosilane;1,3,5,7-tetraoxido-2,4,6,8,9,10-hexaoxa-1,3,5,7-tetrasilatricyclo[3.3.1.13,7]decane;octadecafluoride IUPAC Name Systematic 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 hexadecamagnesium;decasodium;bis(oxidanylidene)silane;1,3,5,7-tetrakis(oxidanidyl)-2,4,6,8,9,10-hexaoxa-1,3,5,7-tetrasilatricyclo[3.3.1.13,7]decane;octadecafluoride IUPAC Name Traditional 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 hexadecamagnesium;decasodium;diketosilane;1,3,5,7-tetraoxido-2,4,6,8,9,10-hexaoxa-1,3,5,7-tetrasilatricyclo[3.3.1.13,7]decane;octadecafluoride InChI Standard 1 1.0.6 InChI iupac.org 2021.10.14 InChI=1S/18FH.16Mg.10Na.6O10Si4.3O2Si/c;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;6*1-11-5-12(2)8-13(3,6-11)10-14(4,7-11)9-12;3*1-3-2/h18*1H;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;/q;;;;;;;;;;;;;;;;;;16*+2;10*+1;6*-4;;;/p-18 InChIKey Standard 1 1.0.6 InChI iupac.org 2021.10.14 AZJYLVAUMGUUBL-UHFFFAOYSA-A Mass Exact 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 2770.668913 Molecular Formula 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 F18Mg16Na10O66Si27 Molecular Weight 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 2775.0 SMILES Canonical 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 [O-][Si]12O[Si]3(O[Si](O1)(O[Si](O2)(O3)[O-])[O-])[O-].[O-][Si]12O[Si]3(O[Si](O1)(O[Si](O2)(O3)[O-])[O-])[O-].[O-][Si]12O[Si]3(O[Si](O1)(O[Si](O2)(O3)[O-])[O-])[O-].[O-][Si]12O[Si]3(O[Si](O1)(O[Si](O2)(O3)[O-])[O-])[O-].[O-][Si]12O[Si]3(O[Si](O1)(O[Si](O2)(O3)[O-])[O-])[O-].[O-][Si]12O[Si]3(O[Si](O1)(O[Si](O2)(O3)[O-])[O-])[O-].O=[Si]=O.O=[Si]=O.O=[Si]=O.[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2] SMILES Isomeric 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 [O-][Si]12O[Si]3(O[Si](O1)(O[Si](O2)(O3)[O-])[O-])[O-].[O-][Si]12O[Si]3(O[Si](O1)(O[Si](O2)(O3)[O-])[O-])[O-].[O-][Si]12O[Si]3(O[Si](O1)(O[Si](O2)(O3)[O-])[O-])[O-].[O-][Si]12O[Si]3(O[Si](O1)(O[Si](O2)(O3)[O-])[O-])[O-].[O-][Si]12O[Si]3(O[Si](O1)(O[Si](O2)(O3)[O-])[O-])[O-].[O-][Si]12O[Si]3(O[Si](O1)(O[Si](O2)(O3)[O-])[O-])[O-].O=[Si]=O.O=[Si]=O.O=[Si]=O.[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[F-].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2] Topological Polar Surface Area 7 E_TPSA 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 988 Weight MonoIsotopic 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 2766.670998 137 0 0 0 0 0 0 0 53 -1