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| | Triphenylsilanol Basic information |
| | Triphenylsilanol Chemical Properties |
| Melting point | 150-153 °C (lit.) | | Boiling point | 389 °C [760mmHg] | | density | 1.13 | | refractive index | 1.628 | | Fp | >200°C | | storage temp. | Inert atmosphere,Room Temperature | | pka | 13.39±0.58(Predicted) | | form | Powder | | color | white | | Water Solubility | reacts | | Sensitive | Air Sensitive | | Hydrolytic Sensitivity | 4: no reaction with water under neutral conditions | | BRN | 985007 | | InChIKey | NLSXASIDNWDYMI-UHFFFAOYSA-N | | CAS DataBase Reference | 791-31-1(CAS DataBase Reference) | | NIST Chemistry Reference | Silanol, triphenyl-(791-31-1) | | EPA Substance Registry System | Silanol, triphenyl- (791-31-1) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 1 | | RTECS | VV4325500 | | F | 21 | | TSCA | Yes | | HS Code | 29310095 |
| | Triphenylsilanol Usage And Synthesis |
| Chemical Properties | White crystal | | Uses | Triphenylsilanol is used as a water surrogate for regioselective Pd catalyzed allylations. A thick on germanium substrates have been produced by the electron bombardment of an evaporated thin film of triphenylsilanol. | | Definition | ChEBI: An organosilanol in which silicon is bonded to a single hydroxy function and to three phenyl groups. | | Purification Methods | It is purified by dissolving in pet ether, passing through an Al2O3 column, eluting thoroughly with CCl4 to remove impurities and then eluting the silanol with MeOH. Evaporation gives crystals with m 153-155o. It can be recrystallised from pet ether, CCl4 or from *benzene or Et2O/pet ether (1:1). It has also been recrystallised by partial freezing from the melt to constant melting point. [George & Gilman J Am Chem Soc 81 3288 1959, IR: Tatlock & Rochow J Org Chem 17 1555 1952 and Richards & Thompson J Chem Soc 124 1949, Beilstein 16 IV 1480.] |
| | Triphenylsilanol Preparation Products And Raw materials |
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