16196127 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 17 8 8 8 8 7 7 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 2 -1 6 1 1 1 1 1 6 6 6 7 7 7 8 8 8 9 10 10 11 11 12 13 13 14 14 15 15 16 16 16 17 17 17 18 18 19 20 21 21 22 22 23 23 24 25 26 26 26 27 27 27 2 3 4 5 9 12 16 21 26 27 9 10 13 14 11 15 12 28 29 18 30 19 31 20 32 33 34 35 20 22 23 19 36 38 37 24 25 24 39 25 40 41 42 43 44 45 46 47 48 1 2 2 2 1 2 1 1 1 1 1 1 2 2 2 1 1 1 1 1 1 1 1 2 1 1 1 1 1 2 1 2 1 1 1 2 1 1 1 2 1 1 1 1 1 1 1 1 1 15 10 32 20 37 17 2 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 8.3516 7.4856 9.2177 7.8516 8.8516 3.2018 4.0678 2.3358 2.3358 3.2018 4.0678 4.0678 1.4418 1.4418 3.2018 3.2018 4.0678 0.5357 0.5357 4.0678 4.0678 3.2018 4.9338 3.2018 4.9338 4.9338 3.2018 4.6047 4.6047 1.449 1.449 2.6648 2.5818 3.2018 3.8218 0 4.6047 0 2.6648 5.4708 2.6648 5.4708 5.2438 5.4708 4.6238 3.5118 2.6648 2.8918 5.0785 4.5785 5.5785 5.9445 4.2124 1.62 9.12 3.12 2.12 3.62 3.12 2.12 3.6547 1.5853 4.62 0.62 6.12 3.1408 2.0992 5.12 8.12 6.62 6.62 7.62 7.62 9.62 9.62 3.43 1.81 4.2746 0.9654 4.93 0.62 0 0.62 3.4529 4.81 1.7871 6.31 6.31 7.93 7.93 9.0831 9.93 10.1569 10.1569 9.93 9.0831 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 6 6 8 8 8 9 10 11 13 14 17 17 18 21 21 22 23 9 12 9 10 13 14 11 12 18 19 22 23 19 24 25 24 25 0 Compound Canonicalized 5 2021.10.14 1 Compound Complexity 7 E_COMPLEXITY 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 464 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 5 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 3 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 00000371E07B38000400000000000000000000000000000000003C6080000000000000B1F400001C00000000000C08C11E043EC0F30C1000A0033467440082802031022008D8203864980820E2C09191842008608000C8C8071080C00E88000000000200001000000000040000000000000000 IUPAC Name Allowed 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 N,N-dimethyl-4-[(E)-2-(1-methylquinolin-1-ium-4-yl)vinyl]aniline;perchlorate IUPAC Name CAS-like Style 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 N,N-dimethyl-4-[(E)-2-(1-methyl-4-quinolin-1-iumyl)ethenyl]aniline;perchlorate IUPAC Name Markup 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 <I>N</I>,<I>N</I>-dimethyl-4-[(<I>E</I>)-2-(1-methylquinolin-1-ium-4-yl)ethenyl]aniline;perchlorate IUPAC Name Preferred 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 N,N-dimethyl-4-[(E)-2-(1-methylquinolin-1-ium-4-yl)ethenyl]aniline;perchlorate IUPAC Name Systematic 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 N,N-dimethyl-4-[(E)-2-(1-methylquinolin-1-ium-4-yl)ethenyl]aniline;perchlorate IUPAC Name Traditional 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.10.14 dimethyl-[4-[(E)-2-(1-methylquinolin-1-ium-4-yl)vinyl]phenyl]amine;perchlorate InChI Standard 1 1.0.6 InChI iupac.org 2021.10.14 InChI=1S/C20H21N2.ClHO4/c1-21(2)18-12-9-16(10-13-18)8-11-17-14-15-22(3)20-7-5-4-6-19(17)20;2-1(3,4)5/h4-15H,1-3H3;(H,2,3,4,5)/q+1;/p-1 InChIKey Standard 1 1.0.6 InChI iupac.org 2021.10.14 XZAVEAMNPDBFQD-UHFFFAOYSA-M Mass Exact 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 388.1189848 Molecular Formula 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 C20H21ClN2O4 Molecular Weight 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 388.8 SMILES Canonical 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 C[N+]1=CC=C(C2=CC=CC=C21)C=CC3=CC=C(C=C3)N(C)C.[O-]Cl(=O)(=O)=O SMILES Isomeric 1 2.3.0 OEChem OpenEye Scientific Software 2021.10.14 C[N+]1=CC=C(C2=CC=CC=C21)/C=C/C3=CC=C(C=C3)N(C)C.[O-]Cl(=O)(=O)=O Topological Polar Surface Area 7 E_TPSA 3.4.8.18 Cactvs Xemistry GmbH 2021.10.14 81.4 Weight MonoIsotopic 1 2.2 PubChem ncbi.nlm.nih.gov 2021.10.14 388.1189848 27 0 0 0 1 1 0 0 2 -1