methanone, phenyl(trimethylsilyl)-
Phenyl(trimethylsilyl)methanone
CAS: 5908-41-8
Molecular Formula: C10H14OSi
methanone, phenyl(trimethylsilyl)- - Names and Identifiers
| Name | Phenyl(trimethylsilyl)methanone |
| Synonyms | Silane, benzoyltrimethyl- phenyl(triMethylsilyl)Methanone Phenyl(trimethylsilyl)methanone Methanone, phenyl(trimethylsilyl)- methanone, phenyl(trimethylsilyl)- |
| CAS | 5908-41-8 |
| InChI | InChI=1/C10H14OSi/c1-12(2,3)10(11)9-7-5-4-6-8-9/h4-8H,1-3H3 |
methanone, phenyl(trimethylsilyl)- - Physico-chemical Properties
| Molecular Formula | C10H14OSi |
| Molar Mass | 178.3 |
| Density | 0.939±0.06 g/cm3(Predicted) |
| Boling Point | 84 °C(Press: 2 Torr) |
| Flash Point | 83.5°C |
| Vapor Presure | 0.155mmHg at 25°C |
| Refractive Index | 1.483 |
methanone, phenyl(trimethylsilyl)- - Introduction
Phenyl(trimethylsilyl)methanone, also known as trimethylsilyl (Phenyl) methanone, is an organic compound. Its chemical formula is C10H16OSi and its molecular weight is 180.32g/mol. The following is a description of the properties, uses, preparation and safety information of this compound:
Nature:
Phenyl(trimethylsilyl)methanone is a colorless to pale yellow liquid with a special aroma. It is soluble in many organic solvents such as ethanol, dimethylformamide and dichloromethane.
Use:
Phenyl(trimethylsilyl)methanone is widely used in organic synthesis. It is an important reagent used to catalyze fluorinated aromatic hydrocarbons, acylation reactions and laziness reactions. In addition, it can also be used as a ligand for transition metal catalysts in organic synthesis.
Preparation Method:
Phenyl(trimethylsilyl)methanone can be synthesized by the reaction of trimethylsilylchloromethane and benzaldehyde. The specific preparation method is as follows:
At low temperature, benzaldehyde is added to trimethylsilylchloromethane, and then slowly warmed to room temperature and stirred for several hours. Finally, the target product was purified by distillation.
Safety Information:
Although there is no specific safety data for Phenyl(trimethylsilyl)methanone, based on the safety of similar compounds, it is recommended to take appropriate protective measures when using this compound. Keep away from fire and heat sources and avoid contact with oxidants. At the same time, it should be used in a well-ventilated area with appropriate protective gloves and goggles. If contact with skin, eyes or inhalation occurs, rinse immediately with plenty of water and seek medical advice.
Nature:
Phenyl(trimethylsilyl)methanone is a colorless to pale yellow liquid with a special aroma. It is soluble in many organic solvents such as ethanol, dimethylformamide and dichloromethane.
Use:
Phenyl(trimethylsilyl)methanone is widely used in organic synthesis. It is an important reagent used to catalyze fluorinated aromatic hydrocarbons, acylation reactions and laziness reactions. In addition, it can also be used as a ligand for transition metal catalysts in organic synthesis.
Preparation Method:
Phenyl(trimethylsilyl)methanone can be synthesized by the reaction of trimethylsilylchloromethane and benzaldehyde. The specific preparation method is as follows:
At low temperature, benzaldehyde is added to trimethylsilylchloromethane, and then slowly warmed to room temperature and stirred for several hours. Finally, the target product was purified by distillation.
Safety Information:
Although there is no specific safety data for Phenyl(trimethylsilyl)methanone, based on the safety of similar compounds, it is recommended to take appropriate protective measures when using this compound. Keep away from fire and heat sources and avoid contact with oxidants. At the same time, it should be used in a well-ventilated area with appropriate protective gloves and goggles. If contact with skin, eyes or inhalation occurs, rinse immediately with plenty of water and seek medical advice.
Last Update：2024-04-10 22:29:15
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