Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C33H49P |
| Molecular Weight | 476.7159 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C1=CC(C(C)C)=C(C(=C1)C(C)C)C2=C(C=CC=C2)P(C3CCCCC3)C4CCCCC4
InChI
InChIKey=UGOMMVLRQDMAQQ-UHFFFAOYSA-N
InChI=1S/C33H49P/c1-23(2)26-21-30(24(3)4)33(31(22-26)25(5)6)29-19-13-14-20-32(29)34(27-15-9-7-10-16-27)28-17-11-8-12-18-28/h13-14,19-25,27-28H,7-12,15-18H2,1-6H3
| Molecular Formula | C33H49P |
| Molecular Weight | 476.7159 |
| 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 |
|---|---|---|
| Dicyclohexyl(2',4',6'-triisopropylbiphenyl-2-yl)phosphine-dichlorophenylborane. | 2009-10-17 |
|
| Palladium catalysed aryl amination reactions in supercritical carbon dioxide. | 2005-10-21 |
|
| Insights into the origin of high activity and stability of catalysts derived from bulky, electron-rich monophosphinobiaryl ligands in the Pd-catalyzed C-N bond formation. | 2003-11-19 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:45:27 GMT 2025
by
admin
on
Mon Mar 31 22:45:27 GMT 2025
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| Record UNII |
R271FU23T8
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| Record Status |
Validated (UNII)
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