| | Identification | More |  | [Name] 
 Triphenylsilanol
 |  | [CAS] 
 791-31-1
 |  | [Synonyms] 
 TRIPHENYLSILANOL
 hydroxytriphenyl-silan
 Silane, (hydroxytriphenyl)-
 Silanol,triphenyl-
 Triphenylhydroxysilane
 triphenyl-silano
 Triphenylsilylhydroxide
 Triphenylsilanolwhitepowder
 TriphenylsilSIT8722.0
 Triphenylsilanol,98%
 Triphenylsilanol,99%
 |  | [EINECS(EC#)] 
 212-339-3
 |  | [Molecular Formula] 
 C18H16OSi
 |  | [MDL Number] 
 MFCD00002102
 |  | [Molecular Weight] 
 276.4
 |  | [MOL File] 
 791-31-1.mol
 | 
 | Chemical Properties | Back Directory |  | [Appearance] 
 White  crystal
 |  | [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
 |  | [form ] 
 Powder
 |  | [pka] 
 13.39±0.58(Predicted)
 |  | [color ] 
 white
 |  | [Water Solubility ] 
 reacts
 |  | [Hydrolytic Sensitivity] 
 4: no reaction with water under neutral conditions
 |  | [Sensitive ] 
 Air Sensitive
 |  | [Detection Methods] 
 HPLC
 |  | [BRN ] 
 985007
 |  | [InChIKey] 
 NLSXASIDNWDYMI-UHFFFAOYSA-N
 |  | [CAS DataBase Reference] 
 791-31-1(CAS DataBase Reference)
 |  | [NIST Chemistry Reference] 
 Silanol, triphenyl-(791-31-1)
 |  | [Storage Precautions] 
 Moisture sensitive
 |  | [EPA Substance Registry System] 
 791-31-1(EPA Substance)
 | 
 | Safety Data | Back Directory |  | [Hazard Codes ] 
 Xi
 |  | [Risk Statements ] 
 R36/37/38:Irritating to eyes, respiratory system and skin .
 |  | [Safety Statements ] 
 S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
 S36:Wear suitable protective clothing .
 |  | [WGK Germany ] 
 1
 
 |  | [RTECS ] 
 VV4325500
 
 |  | [F ] 
 21
 |  | [TSCA ] 
 Yes
 |  | [HS Code ] 
 29310095
 | 
 | Hazard Information | Back Directory |  | [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.]
 | 
 |  |