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Phenylsilane, 97%, Thermo Scientific ChemicalsHave Questions?
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Catalog number A17901.22
also known as A17901-22
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Quantity:
100 g
Chemical Identifiers
CAS694-53-1
IUPAC Namephenylsilyl
Molecular FormulaC6H7Si
InChI KeyJAZKZOWBOMBYIX-UHFFFAOYSA-N
SMILES[SiH2]C1=CC=CC=C1
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Specifications
Specification Sheet
Specification SheetRefractive Index1.5085-1.5135 @ 20°C (U.K. specification)
Appearance (Color)Clear colorless
FormLiquid
Assay (GC)≥96.0% (U.K. specification)
CommentPurchased in U.K. and U.S.
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It is used as a pharmaceutical intermediate.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
It is used as a pharmaceutical intermediate.
Solubility
Contact with water releases a flammable alcohol. Soluble in water (Contact with water releases flammable gases), and most common organic solvents.
Notes
Moisture Sensitive. Store away from water/moisture. Keep the container tightly closed and place it in a cool, dry and well ventilated condition. Protect against electrostatic charges. Keep ignition sources away. Store under inert gas.
It is used as a pharmaceutical intermediate.
Solubility
Contact with water releases a flammable alcohol. Soluble in water (Contact with water releases flammable gases), and most common organic solvents.
Notes
Moisture Sensitive. Store away from water/moisture. Keep the container tightly closed and place it in a cool, dry and well ventilated condition. Protect against electrostatic charges. Keep ignition sources away. Store under inert gas.
RUO – Research Use Only
General References:
- Richard Apodaca and Wei Xiao. Direct Reductive Amination of Aldehydes and Ketones Using Phenylsilane: Catalysis by Dibutyltin Dichloride.Org. Lett.,2001,3(11), 1745-1748.
- John L. Speier.; Ruth Zimmerman.; James Webster. The Addition of Silicon Hydrides to Olefinic Double Bonds. Part I. The Use of Phenylsilane, Diphenylsilane, Phenylmethylsilane, Amylsilane and Tribromosilane.J. Am. Chem. Soc., 1956,78(10), 2278-2281.