Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C11H14O |
| Molecular Weight | 162.2283 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(C)C(=O)C1=CC=CC=C1
InChI
InChIKey=OECPUBRNDKXFDX-UHFFFAOYSA-N
InChI=1S/C11H14O/c1-11(2,3)10(12)9-7-5-4-6-8-9/h4-8H,1-3H3
| Molecular Formula | C11H14O |
| Molecular Weight | 162.2283 |
| 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 |
|---|---|---|
| Rapid ketone transfer hydrogenation by employing simple, in situ prepared iridium(I) precatalysts supported by "non-N--H" P,N ligands. | 2008 |
|
| Regioselective alkenylation of aromatic ketones with alkenylboronates using a RuH2(CO)(PPh3)3 catalyst via carbon-hydrogen bond cleavage. | 2007-04-27 |
|
| New Ru complexes containing the N-tridentate bpea and phosphine ligands: consequences of meridional vs facial geometry. | 2006-12-25 |
|
| A RuH(2)(CO)(PPh(3))(3)-catalyzed regioselective arylation of aromatic ketones with arylboronates via carbon-hydrogen bond cleavage. | 2005-04-27 |
|
| Base-catalyzed hydrogenation: rationalizing the effects of catalyst and substrate structures and solvation. | 2005-03-02 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:05:26 GMT 2025
by
admin
on
Mon Mar 31 21:05:26 GMT 2025
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| Record UNII |
96BA178UNX
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| Record Status |
Validated (UNII)
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| Record Version |
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70308
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96BA178UNX
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DTXSID1048209
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