1.0 2010-04-08 22:15:47 UTC 2019-11-26 03:20:34 UTC FDB021574 Sapidolide A Constituent of Baccaurea sapida (Burmese grape). Sapidolide A is found in fruits. C14H18O5 266.2897 266.115423686 13-ethenyl-1,7-dihydroxy-12-methyl-2,10-dioxatetracyclo[5.4.1.1⁸,¹¹.0⁴,¹²]tridecan-9-one 13-ethenyl-1,7-dihydroxy-12-methyl-2,10-dioxatetracyclo[5.4.1.1⁸,¹¹.0⁴,¹²]tridecan-9-one 182191-87-3 CC12C3CCC1(O)C1C(C=C)C(OC1=O)C2(O)OC3 InChI=1S/C14H18O5/c1-3-8-9-11(15)19-10(8)14(17)12(2)7(6-18-14)4-5-13(9,12)16/h3,7-10,16-17H,1,4-6H2,2H3 OZRZMHKATMSFPV-UHFFFAOYSA-N belongs to the class of organic compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom. Gamma butyrolactones Organic compounds Organoheterocyclic compounds Lactones Gamma butyrolactones Aliphatic heteropolycyclic compounds Carbonyl compounds Carboxylic acid esters Cyclic alcohols and derivatives Hemiacetals Hydrocarbon derivatives Monocarboxylic acids and derivatives Organic oxides Oxacyclic compounds Oxepanes Tertiary alcohols Tetrahydrofurans Alcohol Aliphatic heteropolycyclic compound Carbonyl group Carboxylic acid derivative Carboxylic acid ester Cyclic alcohol Gamma butyrolactone Hemiacetal Hydrocarbon derivative Monocarboxylic acid or derivatives Organic oxide Organic oxygen compound Organooxygen compound Oxacycle Oxepane Tertiary alcohol Tetrahydrofuran logp 0.10 ALOGPS logs -1.17 ALOGPS solubility 1.80e+01 g/l ALOGPS melting_point Mp 147° logp 0.51 ChemAxon pka_strongest_acidic 10.66 ChemAxon pka_strongest_basic -3.4 ChemAxon iupac 13-ethenyl-1,7-dihydroxy-12-methyl-2,10-dioxatetracyclo[5.4.1.1⁸,¹¹.0⁴,¹²]tridecan-9-one ChemAxon average_mass 266.2897 ChemAxon mono_mass 266.115423686 ChemAxon smiles CC12C3CCC1(O)C1C(C=C)C(OC1=O)C2(O)OC3 ChemAxon formula C14H18O5 ChemAxon inchi InChI=1S/C14H18O5/c1-3-8-9-11(15)19-10(8)14(17)12(2)7(6-18-14)4-5-13(9,12)16/h3,7-10,16-17H,1,4-6H2,2H3 ChemAxon inchikey OZRZMHKATMSFPV-UHFFFAOYSA-N ChemAxon polar_surface_area 75.99 ChemAxon refractivity 64.45 ChemAxon polarizability 26.11 ChemAxon rotatable_bond_count 1 ChemAxon acceptor_count 4 ChemAxon donor_count 2 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 20078 Specdb::CMs 47392 Specdb::CMs 171024 Specdb::MsMs 310723 Specdb::MsMs 310724 Specdb::MsMs 310725 Specdb::MsMs 355543 Specdb::MsMs 355544 Specdb::MsMs 355545 Specdb::MsMs 2292561 Specdb::MsMs 2292562 Specdb::MsMs 2292563 Specdb::MsMs 2646606 Specdb::MsMs 2646607 Specdb::MsMs 2646608 Specdb::NmrOneD 47682 Specdb::NmrOneD 47683 Specdb::NmrOneD 47684 Specdb::NmrOneD 47685 Specdb::NmrOneD 47686 Specdb::NmrOneD 47687 Specdb::NmrOneD 47688 Specdb::NmrOneD 47689 Specdb::NmrOneD 47690 Specdb::NmrOneD 47691 Specdb::NmrOneD 47692 Specdb::NmrOneD 47693 Specdb::NmrOneD 47694 Specdb::NmrOneD 47695 Specdb::NmrOneD 47696 Specdb::NmrOneD 47697 Specdb::NmrOneD 47698 Specdb::NmrOneD 47699 Specdb::NmrOneD 47700 Specdb::NmrOneD 47701 HMDB41582 #<Reference:0x000055ce335565e8> Fruits Unknown generic