69003343 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 8 8 8 8 8 8 8 7 7 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 2 2 3 3 4 4 5 5 6 6 7 7 8 8 9 9 9 10 10 10 11 11 11 12 12 12 13 13 14 14 15 15 16 16 17 17 18 18 19 19 20 20 21 21 22 22 11 41 12 42 15 43 16 44 17 45 18 46 21 47 22 48 13 19 35 14 20 36 13 15 23 14 16 24 21 25 22 26 17 27 18 28 19 29 20 30 31 32 33 34 37 38 39 40 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 11 1 15 13 23 2 1 12 2 16 14 24 2 1 13 9 11 21 25 1 1 14 10 12 22 26 1 1 15 3 11 17 27 1 1 16 4 12 18 28 1 1 17 5 15 19 29 1 1 18 6 16 20 30 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 4.001 4.001 2.269 2.269 0.5369 0.5369 4.001 4.001 2.269 2.269 3.135 3.135 3.135 3.135 2.269 2.269 1.403 1.403 1.403 1.403 4.001 4.001 3.672 3.135 3.135 3.135 2.8059 1.732 0.866 1.403 0.7924 1.1909 0.7924 1.1909 2.269 2.269 4.6116 4.2131 4.6116 4.2131 4.001 4.001 1.732 1.732 0 0 4.538 4.538 9.93 3.31 10.93 4.31 9.93 3.31 6.93 0.31 7.93 1.31 9.43 2.81 8.43 1.81 9.93 3.31 9.43 2.81 8.43 1.81 7.93 1.31 9.12 3.43 7.81 1.19 10.24 3.62 9.12 3.43 8.5377 7.8474 1.9177 1.2274 7.31 0.69 7.8223 8.5126 1.2023 1.8926 10.55 3.93 11.24 4.62 9.62 3 6.62 0 6 6 5 5 5 5 5 5 11 12 13 14 15 16 17 18 1 2 21 22 3 4 5 6 0 Compound Canonicalized 5 2019.01.04 1 Compound Complexity 7 E_COMPLEXITY 3.4.6.11 Cactvs xemistry.com 2019.06.18 132 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.4.6.11 Cactvs xemistry.com 2019.06.18 10 Count Hydrogen Bond Donor 5 E_NHDONORS 3.4.6.11 Cactvs xemistry.com 2019.06.18 10 Count Rotatable Bond 5 E_NROTBONDS 3.4.6.11 Cactvs xemistry.com 2019.06.18 2 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.4.6.11 Cactvs xemistry.com 2019.06.18 00000371E0733C000000000000000000000000000000000000002C5800000000000000000000001E0010080000083CE18006000002C00200000000000000000000000000000080080000031002008000044000071000910001F060040000000000000000000000000000000000000000000000 IUPAC Name Allowed 1 2.6.6 LexiChem openeye.com 2019.06.18 (2R,3R,4R,5R)-2-(hydroxymethyl)piperidine-3,4,5-triol IUPAC Name CAS-like Style 1 2.6.6 LexiChem openeye.com 2019.06.18 (2R,3R,4R,5R)-2-(hydroxymethyl)piperidine-3,4,5-triol IUPAC Name Markup 1 2.6.6 LexiChem openeye.com 2019.06.18 (2<I>R</I>,3<I>R</I>,4<I>R</I>,5<I>R</I>)-2-(hydroxymethyl)piperidine-3,4,5-triol IUPAC Name Preferred 1 2.6.6 LexiChem openeye.com 2019.06.18 (2R,3R,4R,5R)-2-(hydroxymethyl)piperidine-3,4,5-triol IUPAC Name Systematic 1 2.6.6 LexiChem openeye.com 2019.06.18 (2R,3R,4R,5R)-2-(hydroxymethyl)piperidine-3,4,5-triol IUPAC Name Traditional 1 2.6.6 LexiChem openeye.com 2019.06.18 (2R,3R,4R,5R)-2-methylolpiperidine-3,4,5-triol InChI Standard 1 1.0.5 InChI iupac.org 2019.06.18 InChI=1S/2C6H13NO4/c2*8-2-3-5(10)6(11)4(9)1-7-3/h2*3-11H,1-2H2/t2*3-,4-,5-,6-/m11/s1 InChIKey Standard 1 1.0.5 InChI iupac.org 2019.06.18 BIGCUVTZTSNKQJ-KZXKDKCNSA-N Mass Exact 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 326.16891579 Molecular Formula 1 2.1 PubChem ncbi.nlm.nih.gov 2019.06.18 C12H26N2O8 Molecular Weight 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 326.34 SMILES Canonical 1 2.1.5 OEChem openeye.com 2019.06.18 C1C(C(C(C(N1)CO)O)O)O.C1C(C(C(C(N1)CO)O)O)O SMILES Isomeric 1 2.1.5 OEChem openeye.com 2019.06.18 C1[C@H]([C@H]([C@@H]([C@H](N1)CO)O)O)O.C1[C@H]([C@H]([C@@H]([C@H](N1)CO)O)O)O Topological Polar Surface Area 7 E_TPSA 3.4.6.11 Cactvs xemistry.com 2019.06.18 186 Weight MonoIsotopic 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 326.16891579 22 8 8 0 0 0 0 0 2 -1