(E)-5-Hydroxy-2-isopropenyl-5-methylhex-3-enyl 3-methylbutyrate
PubChem CID: 6429165
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| Compound Synonyms | (E)-5-Hydroxy-2-isopropenyl-5-methylhex-3-enyl 3-methylbutyrate, GEUJVWYWFCONDI-BQYQJAHWSA-N |
|---|---|
| Ghose Rule | True |
| Classyfire Kingdom | Organic compounds |
| Topological Polar Surface Area | 46.5 |
| Hydrogen Bond Donor Count | 1.0 |
| Pfizer 3 75 Rule | False |
| Np Classifier Class | Acyclic monoterpenoids |
| Deep Smiles | CCCC=O)OCCC=C)C))/C=C/CO)C)C)))))))))C |
| Heavy Atom Count | 18.0 |
| Classyfire Class | Fatty acyls |
| Classyfire Subclass | Fatty acid esters |
| Isotope Atom Count | 0.0 |
| Molecular Complexity | 314.0 |
| Database Name | imppat_phytochem;pubchem |
| Defined Atom Stereocenter Count | 0.0 |
| Iupac Name | [(E)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhex-3-enyl] 3-methylbutanoate |
| Veber Rule | True |
| Classyfire Superclass | Lipids and lipid-like molecules |
| Xlogp | 3.3 |
| Gsk 4 400 Rule | True |
| Molecular Formula | C15H26O3 |
| Inchi Key | GEUJVWYWFCONDI-BQYQJAHWSA-N |
| Silicos It Class | Soluble |
| Rotatable Bond Count | 8.0 |
| Synonyms | (e)-5-hydroxy-2-isopropenyl-5-methylhex-3-enyl 3-methylbutyrate |
| Esol Class | Soluble |
| Functional Groups | C/C=C/C, C=C(C)C, CO, COC(C)=O |
| Compound Name | (E)-5-Hydroxy-2-isopropenyl-5-methylhex-3-enyl 3-methylbutyrate |
| Exact Mass | 254.188 |
| Formal Charge | 0.0 |
| Monoisotopic Mass | 254.188 |
| Hydrogen Bond Acceptor Count | 3.0 |
| Molecular Weight | 254.36 |
| Gi Absorption | True |
| Covalent Unit Count | 1.0 |
| Total Atom Stereocenter Count | 1.0 |
| Total Bond Stereocenter Count | 1.0 |
| Lipinski Rule Of 5 | True |
| Inchi | InChI=1S/C15H26O3/c1-11(2)9-14(16)18-10-13(12(3)4)7-8-15(5,6)17/h7-8,11,13,17H,3,9-10H2,1-2,4-6H3/b8-7+ |
| Smiles | CC(C)CC(=O)OCC(/C=C/C(C)(C)O)C(=C)C |
| Np Classifier Biosynthetic Pathway | Terpenoids |
| Defined Bond Stereocenter Count | 1.0 |
| Egan Rule | True |
| Np Classifier Superclass | Monoterpenoids |
- 1. Outgoing r'ship
FOUND_INto/from Ajania Fruticulosa (Plant) Rel Props:Reference:https://doi.org/10.1002/(sici)1099-1026(199903/04)14:2<112::aid-ffj786>3.0.co;2-1