Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C18H16OSi |
| Molecular Weight | 276.4045 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O[Si](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3
InChI
InChIKey=NLSXASIDNWDYMI-UHFFFAOYSA-N
InChI=1S/C18H16OSi/c19-20(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15,19H
| Molecular Formula | C18H16OSi |
| Molecular Weight | 276.4045 |
| 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 |
|---|---|---|
| Determination of fluoride as fluorosilane derivative using reversed-phase HPLC with UV detection for determination of total organic fluorine. | 2010-09 |
|
| Protecting-group-free and catalysis-based total synthesis of the ecklonialactones. | 2010-08-18 |
|
| tert-Butoxy-triphenyl-silane. | 2010-01-27 |
|
| The role of outer-sphere surface acidity in alkene epoxidation catalyzed by calixarene-Ti(IV) complexes. | 2007-12-19 |
|
| 1-Hydr-oxy-1,1,3,3,3-penta-phenyl-disiloxane, [Si(2)O(OH)(Ph)(5)], at 100 K. | 2007-12-12 |
|
| Synthesis and characterization of complexes containing Ti-O-Si moieties. Catalytic activity in olefin epoxidation. | 2007-02-28 |
|
| Hydrogen-bonded adducts of triphenylsilanol with diamines: a finite ten-molecule aggregate, and chain, sheet and framework structures built from O-H...O, O-H...N and C-H...pi(arene) hydrogen bonds. | 2004-04 |
|
| The 1:1 adduct of triphenylsilanol and 4,4'-bipyridyl, and three pairwise-concomitant triclinic polymorphs of the 4:1 adduct having Z' = 0.5, 1 and 4. | 2003-04 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:24:52 GMT 2025
by
admin
on
Mon Mar 31 22:24:52 GMT 2025
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| Record UNII |
AZC8O4TTX4
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| Record Status |
Validated (UNII)
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| Record Version |
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