Identification | More | [Name]
Dimethylphenylsilane | [CAS]
766-77-8 | [Synonyms]
ACETATE BUFFER ACETATE BUFFER, PH 3.5 ACETATE BUFFER, PH 4.0 ACETATE BUFFER, PH 4.5 ACETATE BUFFER, PH 6.0 ACETATE BUFFER REAGENT ACETATE BUFFER SOLUTION R-455 ACETATE BUFFER SOLUTION TYPE 'C' ACETATE BUFFER TS ACETIC ACID-SODIUM ACETATE BUFFER ACETATE BUFFER ACETATE, PH 4.00 BUFFER, PH 4.63 BUFFER PH 4.65 BUFFER PH7.20 BUFFER SOLUTION BUFFER SOLUTION (ACETATE), PH 4.00 BUFFER SOLUTION (ACETATE), PH 4.0-4.5 BUFFER SOLUTION, PH 4.0, ACETATE BUFFER SOLUTION, PH 4.63 | [EINECS(EC#)]
212-170-5 | [Molecular Formula]
C4H7NaO4 | [MDL Number]
MFCD00137248 | [Molecular Weight]
142.09 | [MOL File]
766-77-8.mol |
Chemical Properties | Back Directory | [Appearance]
Clear colorless liquid | [Melting point ]
323-329 °C(lit.) | [Boiling point ]
157 °C744 mm Hg(lit.) | [density ]
0.889 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.497(lit.)
| [Fp ]
95 °F
| [storage temp. ]
2-8°C
| [solubility ]
sol common organic solvent such as chloroform, 1,2-
dichloroethane, benzene, ether, acetone, dioxane, THF; insol
H2O. | [form ]
solid
| [Specific Gravity]
0.889 | [Water Solubility ]
Not miscible in water. | [Hydrolytic Sensitivity]
3: reacts with aqueous base | [BRN ]
2204906 | [InChIKey]
ZISUALSZTAEPJH-UHFFFAOYSA-N | [CAS DataBase Reference]
766-77-8(CAS DataBase Reference) | [EPA Substance Registry System]
Silane, dimethylphenyl- (766-77-8) |
Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R10:Flammable. R36:Irritating to the eyes. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/39:Wear suitable protective clothing and eye/face protection . | [RIDADR ]
UN 1993 3/PG 3
| [WGK Germany ]
1
| [RTECS ]
AJ4375000
| [TSCA ]
Yes | [HazardClass ]
3 | [PackingGroup ]
III | [HS Code ]
29319090 |
Hazard Information | Back Directory | [Chemical Properties]
Clear colorless liquid | [Physical properties]
bp 157 °C/744 mmHg; d 0.889 g cm?3. | [Uses]
Reagent for enol ether synthesis. | [Uses]
Diastereoselective Reduction of Carbonyl Compounds.
Hydrosilylation. With a transition metal catalyst, the
hydrosilane adds to carbon–carbon double or triple bonds to
give alkylsilanes or alkenylsilanes.
Hydrosilylating reagent; reductant in combination with acid
or F?). | [Uses]
Dimethylphenylsilane is a reagent for enol ether synthesis. It acts as a catalyst. Also used as a precursor in Optical Emission Spectroscopy of Plasma Deposition Processes. It can react with vinylbenzene to produce (b-Phenyl-ethyl)-dimethylphenyl-silan. |
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