| Weight | 276.411 g/mol |
|---|---|
| Formula | C18H16OSi |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 3 |
Triphenylsilanol (791-31-1)
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- The Reactions of Triphenylsilanol and Diphenylsilanediol with Some Titanium Esters1 (Journal of the American Chemical Society, 1957)
- Triphenylsilanol as a water surrogate for regioselective Pd catalyzed allylations (Tetrahedron Letters, 1993)
- The acid strength of triphenylsilanol (Journal of Inorganic and Nuclear Chemistry, 1958)
- Reactivity Studies of a Stable N-Heterocyclic Silylene with Triphenylsilanol and Pentafluorophenol (Organometallics, 2012)
- 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 (Acta Crystallographica Section B-structural Science, 2003)
- Protonation of chromium tricarbonyl complexes of triphenylsilanol and triphenylcarbinol: synthetic, x-ray crystallographic, and NMR study of (Ph3SiOH)[Cr(CO)3]n (n = 1-3) and of (Ph3COH)Cr(CO)3 (Organometallics, 1993)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC1=CC=C(C=C1)[Si](C2=CC=CC=C2)(C3=CC=CC=C3)O
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InChIKeyNLSXASIDNWDYMI-UHFFFAOYSA-N
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Triphenylsilanol
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