51111338 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 17 16 7 7 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 2 2 3 3 3 4 4 5 5 5 5 6 6 6 7 7 7 8 8 9 9 11 11 11 12 12 13 14 14 15 15 16 16 17 17 18 19 18 10 13 8 9 11 10 12 6 7 10 20 8 21 22 9 23 24 25 26 27 28 14 29 30 13 15 16 17 31 18 32 19 33 35 36 19 34 1 1 1 1 1 1 2 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 2 1 1 2 1 2 1 2 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 2 5.5443 9.1279 5.5443 7.1279 7.6279 7.6279 8.6279 8.6279 6.1279 10.1279 4.5981 4.5981 10.6279 3.732 3.732 11.6279 2.866 2.866 6.8179 7.7356 7.0453 7.0453 7.7356 9.2105 8.5202 8.5202 9.2105 10.7105 10.0202 10.3179 3.732 3.732 2.3291 11.9379 11.9379 1 -0.8047 0 0.8047 -0 0.866 -0.866 0.866 -0.866 -0 0 0.5 -0.5 -0.866 1 -1 -0.866 0.5 -0.5 -0.5369 1.4766 1.0781 -1.0781 -1.4766 1.0781 1.4766 -1.4766 -1.0781 0.2121 0.6106 -1.403 1.62 -1.62 -0.81 -1.403 -0.3291 8 8 8 8 8 8 8 8 8 8 2 2 4 4 12 12 13 15 16 18 10 13 10 12 13 15 16 18 19 19 0 Compound Canonicalized 5 2019.01.04 1 Compound Complexity 7 E_COMPLEXITY 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 317 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 3 Count Hydrogen Bond Donor 5 E_NHDONORS 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 0 Count Rotatable Bond 5 E_NROTBONDS 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 3 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 00000371E07300004400000000000000000000000001600000003C400000000000005801F000001C06000000000D0AC1562430C1B3081008A4012462440083F0A0610F3848983C3866980820A2E19391842008608000E8C8071000000A00020000020001000004000004000200000000000000 IUPAC Name Allowed 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 2-(1-allyl-4-piperidyl)-5-chloro-1,3-benzothiazole IUPAC Name CAS-like Style 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 5-chloro-2-(1-prop-2-enyl-4-piperidinyl)-1,3-benzothiazole IUPAC Name Markup 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 5-chloro-2-(1-prop-2-enylpiperidin-4-yl)-1,3-benzothiazole IUPAC Name Preferred 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 5-chloro-2-(1-prop-2-enylpiperidin-4-yl)-1,3-benzothiazole IUPAC Name Systematic 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 5-chloranyl-2-(1-prop-2-enylpiperidin-4-yl)-1,3-benzothiazole IUPAC Name Traditional 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 2-(1-allyl-4-piperidyl)-5-chloro-1,3-benzothiazole InChI Standard 1 1.0.6 InChI iupac.org 2021.05.07 InChI=1S/C15H17ClN2S/c1-2-7-18-8-5-11(6-9-18)15-17-13-10-12(16)3-4-14(13)19-15/h2-4,10-11H,1,5-9H2 InChIKey Standard 1 1.0.6 InChI iupac.org 2021.05.07 RUSZNMHTAYVDIR-UHFFFAOYSA-N Log P XLogP3-AA 7 3.0 sioc-ccbg.ac.cn 2021.05.07 4.3 Mass Exact 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 292.0800974 Molecular Formula 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 C15H17ClN2S Molecular Weight 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 292.8 SMILES Canonical 1 2.3.0 OEChem OpenEye Scientific Software 2021.05.07 C=CCN1CCC(CC1)C2=NC3=C(S2)C=CC(=C3)Cl SMILES Isomeric 1 2.3.0 OEChem OpenEye Scientific Software 2021.05.07 C=CCN1CCC(CC1)C2=NC3=C(S2)C=CC(=C3)Cl Topological Polar Surface Area 7 E_TPSA 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 44.4 Weight MonoIsotopic 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 292.0800974 19 0 0 0 0 0 0 0 1 -1