EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C15H24O |
| Net Charge | 0 |
| Average Mass | 220.356 |
| Monoisotopic Mass | 220.18272 |
| SMILES | CC1CCC2C3(C)CC4CC12CCC4(C)O3 |
| InChI | InChI=1S/C15H24O/c1-10-4-5-12-14(3)8-11-9-15(10,12)7-6-13(11,2)16-14/h10-12H,4-9H2,1-3H3 |
| InChIKey | HWFDBJBIXBKOLG-UHFFFAOYSA-N |
| Roles Classification |
|---|
| Chemical Role: | polar aprotic solvent A solvent with a comparatively high relative permittivity (or dielectric constant), greater than ca. 15, and a sizable permanent dipole moment, that cannot donate suitably labile hydrogen atoms to form strong hydrogen bonds. |
| Application: | polar aprotic solvent A solvent with a comparatively high relative permittivity (or dielectric constant), greater than ca. 15, and a sizable permanent dipole moment, that cannot donate suitably labile hydrogen atoms to form strong hydrogen bonds. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| 2,6,9-trimethyl-13-oxatetracyclo[6.3.1.16,9.01,5]tridecane (CHEBI:194089) is a oxolane (CHEBI:26911) |
| Incoming Relation(s) |
| 2,6,9-trimethyl-13-oxatetracyclo[6.3.1.16,9.01,5]tridecane carbocation (CHEBI:195527) has functional parent 2,6,9-trimethyl-13-oxatetracyclo[6.3.1.16,9.01,5]tridecane (CHEBI:194089) |
| UniProt Name | Source |
|---|---|
| 2,6,9-trimethyl-13-oxatetracyclo[6.3.1.16,9.01,5]tridecane | UniProt |
| Citations |
|---|