1.0 2010-04-08 22:05:21 UTC 2019-11-26 02:57:23 UTC FDB002380 Cyclolaudenyl palmitate Isolated from corn pollen (Zea mays). Cyclolaudenyl palmitate is found in cereals and cereal products and fats and oils. C47H82O2 679.1528 678.631481868 15-(5,6-dimethylhept-6-en-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl hexadecanoate 15-(5,6-dimethylhept-6-en-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl hexadecanoate 104109-19-5 CCCCCCCCCCCCCCCC(=O)OC1CCC23CC22CCC4(C)C(CCC4(C)C2CCC3C1(C)C)C(C)CCC(C)C(C)=C InChI=1S/C47H82O2/c1-10-11-12-13-14-15-16-17-18-19-20-21-22-23-42(48)49-41-29-31-46-34-47(46)33-32-44(8)38(37(5)25-24-36(4)35(2)3)28-30-45(44,9)40(47)27-26-39(46)43(41,6)7/h36-41H,2,10-34H2,1,3-9H3 JRXHHEVIGCDJBO-UHFFFAOYSA-N belongs to the class of organic compounds known as cycloartanols and derivatives. These are steroids containing a cycloartanol moiety. Cycloartanols and derivatives Organic compounds Lipids and lipid-like molecules Steroids and steroid derivatives Cycloartanols and derivatives Aliphatic homopolycyclic compounds Carbonyl compounds Carboxylic acid esters Fatty acid esters Hydrocarbon derivatives Monocarboxylic acids and derivatives Organic oxides Steroid esters Triterpenoids 9b,19-cyclo-lanostane-skeleton Aliphatic homopolycyclic compound Carbonyl group Carboxylic acid derivative Carboxylic acid ester Cycloartane-skeleton Cycloartanol-skeleton Fatty acid ester Fatty acyl Hydrocarbon derivative Monocarboxylic acid or derivatives Organic oxide Organic oxygen compound Organooxygen compound Steroid ester Triterpenoid logp 10.61 ALOGPS logs -7.60 ALOGPS solubility 1.71e-05 g/l ALOGPS logp 14.81 ChemAxon pka_strongest_basic -7 ChemAxon iupac 15-(5,6-dimethylhept-6-en-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl hexadecanoate ChemAxon average_mass 679.1528 ChemAxon mono_mass 678.631481868 ChemAxon smiles CCCCCCCCCCCCCCCC(=O)OC1CCC23CC22CCC4(C)C(CCC4(C)C2CCC3C1(C)C)C(C)CCC(C)C(C)=C ChemAxon formula C47H82O2 ChemAxon inchi InChI=1S/C47H82O2/c1-10-11-12-13-14-15-16-17-18-19-20-21-22-23-42(48)49-41-29-31-46-34-47(46)33-32-44(8)38(37(5)25-24-36(4)35(2)3)28-30-45(44,9)40(47)27-26-39(46)43(41,6)7/h36-41H,2,10-34H2,1,3-9H3 ChemAxon inchikey JRXHHEVIGCDJBO-UHFFFAOYSA-N ChemAxon polar_surface_area 26.3 ChemAxon refractivity 209.1 ChemAxon polarizability 90.94 ChemAxon rotatable_bond_count 21 ChemAxon acceptor_count 1 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 19543 Specdb::MsMs 88578 Specdb::MsMs 88579 Specdb::MsMs 88580 Specdb::MsMs 151332 Specdb::MsMs 151333 Specdb::MsMs 151334 Specdb::MsMs 2447568 Specdb::MsMs 2447569 Specdb::MsMs 2447570 Specdb::MsMs 2518908 Specdb::MsMs 2518909 Specdb::MsMs 2518910 HMDB30508 #<Reference:0x000055ce324271a0> Breakfast cereal Type 2 specific Cereals and cereal products Unknown generic Fats and oils Unknown generic