Trimethoxy(pentafluorophenyl)silane
trimethoxy(pentafluorophenyl)silane
CAS: 223668-64-2
Molecular Formula: C9H9F5O3Si
Trimethoxy(pentafluorophenyl)silane - Names and Identifiers
| Name | trimethoxy(pentafluorophenyl)silane |
| Synonyms | PENTAFLUOROPHENYLTRIMETHOXYSILANE Trimethoxy(perfluorophenyl)silane trimethoxy(pentafluorophenyl)silane Trimethoxy(pentafluorophenyl)silane TRIMETHOXY(PENTAFLUOROPHENYL)SILANE Trimethoxy-(2,3,4,5,6-Pentafluorophenyl)Silane Benzene,1,2,3,4,5-pentafluoro-6-(trimethoxysilyl)- benzene, 1,2,3,4,5-pentafluoro-6-(trimethoxysilyl)- |
| CAS | 223668-64-2 |
| InChI | InChI=1/C9H9F5O3Si/c1-15-18(16-2,17-3)9-7(13)5(11)4(10)6(12)8(9)14/h1-3H3 |
Trimethoxy(pentafluorophenyl)silane - Physico-chemical Properties
| Molecular Formula | C9H9F5O3Si |
| Molar Mass | 288.24 |
| Density | 1.373 |
| Boling Point | 184.5±40.0 °C(Predicted) |
| Flash Point | 65.4°C |
| Vapor Presure | 1mmHg at 25°C |
| Appearance | clear liquid |
| Specific Gravity | 1.373 |
| Color | Colorless to Almost colorless |
| Storage Condition | Room Temprature |
| Sensitive | 7: reacts slowly with moisture/water |
| Refractive Index | 1.4160 to 1.4200 |
Trimethoxy(pentafluorophenyl)silane - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Hazard Note | Irritant |
Trimethoxy(pentafluorophenyl)silane - Introduction
trimethoxy(pentafluorophenyl)silane is an organosilicon compound with the formula C9H11F5O3Si. The following is an introduction to some properties, applications, preparation methods and safety information about trimethoxy(pentafluorophenyl)silane:
Nature:
-Appearance: trimethoxy(pentafluorophenyl)silane is a colorless and transparent liquid.
-Solubility: It is soluble in many organic solvents, such as methanol, ethanol, ethers and aromatic hydrocarbons.
-Stability: trimethoxy(pentafluorophenyl)silane is a stable compound that is not easy to decompose at room temperature.
Use:
trimethoxy(pentafluorophenyl)silane has many applications in organic synthesis:
-As a ligand in organometallic catalysts, it participates in chemical reactions and catalyzes the formation of carbon-carbon bonds and carbon-silicon bonds.
-As a transition metal catalyst and catalyst precursor in organic synthesis, used to build complex organic molecules.
-It can be used as a surface treatment agent to improve the wear resistance and lubricity of the material.
-In materials science, it can be used to improve the surface wettability and adhesion of polymers.
Preparation Method:
The preparation of trimethoxy(pentafluorophenyl)silane usually uses the typical reaction of organosilicon compounds, such:
Hydroquinone reacts with pentafluorobenzoyl fluoride to generate the corresponding acid chloride compound, and then reacts with trimethoxysilanol to obtain trimethoxy(pentafluorophenyl)silane.
Safety Information:
- trimethoxy (pentafluophenyl) silane has a high viscosity. Pay attention to avoid skin and eye contact when using it.
-Provide adequate ventilation during use to avoid inhalation of vapors.
-If you accidentally inhale or come into contact with trimethoxy(pentafluorophenyl)silane, immediately move the patient to a fresh air and seek medical assistance.
-During storage and handling, care should be taken to avoid contact with strong oxidants and strong acids to avoid dangerous reactions.
Nature:
-Appearance: trimethoxy(pentafluorophenyl)silane is a colorless and transparent liquid.
-Solubility: It is soluble in many organic solvents, such as methanol, ethanol, ethers and aromatic hydrocarbons.
-Stability: trimethoxy(pentafluorophenyl)silane is a stable compound that is not easy to decompose at room temperature.
Use:
trimethoxy(pentafluorophenyl)silane has many applications in organic synthesis:
-As a ligand in organometallic catalysts, it participates in chemical reactions and catalyzes the formation of carbon-carbon bonds and carbon-silicon bonds.
-As a transition metal catalyst and catalyst precursor in organic synthesis, used to build complex organic molecules.
-It can be used as a surface treatment agent to improve the wear resistance and lubricity of the material.
-In materials science, it can be used to improve the surface wettability and adhesion of polymers.
Preparation Method:
The preparation of trimethoxy(pentafluorophenyl)silane usually uses the typical reaction of organosilicon compounds, such:
Hydroquinone reacts with pentafluorobenzoyl fluoride to generate the corresponding acid chloride compound, and then reacts with trimethoxysilanol to obtain trimethoxy(pentafluorophenyl)silane.
Safety Information:
- trimethoxy (pentafluophenyl) silane has a high viscosity. Pay attention to avoid skin and eye contact when using it.
-Provide adequate ventilation during use to avoid inhalation of vapors.
-If you accidentally inhale or come into contact with trimethoxy(pentafluorophenyl)silane, immediately move the patient to a fresh air and seek medical assistance.
-During storage and handling, care should be taken to avoid contact with strong oxidants and strong acids to avoid dangerous reactions.
Last Update：2024-04-10 22:29:15
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View History
Trimethoxy(pentafluorophenyl)silane
二环己基胺(S)-2,4-双((叔丁氧基羰基)氨基)丁酸甲酯
Bis(hexamethylenetriaminepenta(methylenephosphonic acid))
Chlorotri(1-pyrrolidinyl)phosphonium hexafluorophosphate
(2-溴-3-吡啶基)氨基甲酸叔丁酯
lithiumdihydrogenorthophosphate
1-HYDROXYETHYLIDENEDI (PHOSPHONIC ACID)
Silane, trimethyl[(2-methyl-2-propenyl)oxy]-
6-溴-5-羟基-1-甲基-2-苯硫甲基吲哚-3-甲酸乙酯
TRANS-T-BUTYL-4-HYDROXYCYCLOHEXYLCARBAMATE
二环己基胺(S)-2,4-双((叔丁氧基羰基)氨基)丁酸甲酯
Bis(hexamethylenetriaminepenta(methylenephosphonic acid))
Chlorotri(1-pyrrolidinyl)phosphonium hexafluorophosphate
(2-溴-3-吡啶基)氨基甲酸叔丁酯
lithiumdihydrogenorthophosphate
1-HYDROXYETHYLIDENEDI (PHOSPHONIC ACID)
Silane, trimethyl[(2-methyl-2-propenyl)oxy]-
6-溴-5-羟基-1-甲基-2-苯硫甲基吲哚-3-甲酸乙酯
TRANS-T-BUTYL-4-HYDROXYCYCLOHEXYLCARBAMATE