Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H22O |
| Molecular Weight | 206.3239 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(C)C1=CC(=CC(O)=C1)C(C)(C)C
InChI
InChIKey=ZDWSNKPLZUXBPE-UHFFFAOYSA-N
InChI=1S/C14H22O/c1-13(2,3)10-7-11(14(4,5)6)9-12(15)8-10/h7-9,15H,1-6H3
| Molecular Formula | C14H22O |
| Molecular Weight | 206.3239 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Combining the benefits of homogeneous and heterogeneous catalysis with tunable solvents and nearcritical water. | 2010-11-16 |
|
| Combining homogeneous catalysis with heterogeneous separation using tunable solvent systems. | 2010-03-25 |
|
| Photoinduced energy transfer processes within dyads of metallophthalocyanines compactly fused to a ruthenium(II) polypyridine chromophore. | 2007-09-28 |
|
| Models for the molybdenum hydroxylases: synthesis, characterization and reactivity of cis-oxosulfido-Mo(VI) complexes. | 2006-01-11 |
|
| Dye-sensitized photooxygenation of the C=N bond. 5. substituent effects on the cleavage of the C=N bond of C-aryl-N-aryl-N-methylhydrazones. | 2005-05-27 |
|
| [Determination of 2,4,6-tri-tert-butylphenol and related compounds in foods]. | 2001-12 |
|
| Autoxidation of substituted phenols catalyzed by cobalt Schiff base complexes in supercritical carbon dioxide. | 2001-07-02 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:14:43 GMT 2025
by
admin
on
Mon Mar 31 19:14:43 GMT 2025
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| Record UNII |
F4SMH8G9W7
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| Record Status |
Validated (UNII)
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| Record Version |
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214-513-4
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