1.0 2026-09-22 08:02:01 UTC 2026-09-22 08:02:01 UTC FDB117932 Trimethylsilyl-meso-inositol trimethyl-[2,3,4,5,6-pentakis(trimethylsilyloxy)cyclohexoxy]silane trimethyl-[2,3,4,5,6-pentakis(trimethylsilyloxy)cyclohexyl]oxysilane C24H60O6Si6 613.248 612.300548862 trimethyl({2,3,4,5,6-pentakis[(trimethylsilyl)oxy]cyclohexyl}oxy)silane trimethyl({2,3,4,5,6-pentakis[(trimethylsilyl)oxy]cyclohexyl}oxy)silane C[Si](C)(C)OC1C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C InChI=1S/C24H60O6Si6/c1-31(2,3)25-19-20(26-32(4,5)6)22(28-34(10,11)12)24(30-36(16,17)18)23(29-35(13,14)15)21(19)27-33(7,8)9/h19-24H,1-18H3 FRTKXRNTVMCAKI-UHFFFAOYSA-N belongs to the class of organic compounds known as cyclitols and derivatives. Cyclitols and derivatives are compounds containing a cycloalkane moiety with one hydroxyl group on each of three or more ring atoms. These of also include derivatives where the hydrogen atom of one or more of the hydroxyl groups is replaced with another atom. Cyclitols and derivatives Organic compounds Organic oxygen compounds Organooxygen compounds Alcohols and polyols Aliphatic homomonocyclic compounds Hydrocarbon derivatives Organic metalloid salts Silyl ethers Trialkylheterosilanes Aliphatic homomonocyclic compound Cyclitol or derivatives Hydrocarbon derivative Organic metalloid salt Organic salt Organoheterosilane Organosilicon compound Silyl ether Trialkylheterosilane logp 5.40 ALOGPS logs -6.76 ALOGPS solubility 1.07e-04 g/l ALOGPS logp 8.78 ChemAxon pka_strongest_basic -3.2 ChemAxon iupac trimethyl({2,3,4,5,6-pentakis[(trimethylsilyl)oxy]cyclohexyl}oxy)silane ChemAxon average_mass 613.248 ChemAxon mono_mass 612.300548862 ChemAxon smiles C[Si](C)(C)OC1C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C ChemAxon formula C24H60O6Si6 ChemAxon inchi InChI=1S/C24H60O6Si6/c1-31(2,3)25-19-20(26-32(4,5)6)22(28-34(10,11)12)24(30-36(16,17)18)23(29-35(13,14)15)21(19)27-33(7,8)9/h19-24H,1-18H3 ChemAxon inchikey FRTKXRNTVMCAKI-UHFFFAOYSA-N ChemAxon polar_surface_area 55.38 ChemAxon refractivity 132.53 ChemAxon polarizability 64.91 ChemAxon rotatable_bond_count 12 ChemAxon acceptor_count 6 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon