2-Acetoxymethyl-3-(trimethylsilyl)propene - Names and Identifiers
2-Acetoxymethyl-3-(trimethylsilyl)propene - Physico-chemical Properties
Molecular Formula | C9H18O2Si
|
Molar Mass | 186.32 |
Density | 0.877g/mLat 25°C(lit.) |
Boling Point | 95°C7mm Hg(lit.) |
Flash Point | 160°F |
Water Solubility | reacts |
Solubility | Solubility most organic solvents. |
Vapor Presure | 0.074mmHg at 25°C |
Appearance | Liquid |
Color | Clear colorless |
BRN | 1933657 |
Storage Condition | Inert atmosphere,2-8°C |
Refractive Index | n20/D 1.440(lit.) |
2-Acetoxymethyl-3-(trimethylsilyl)propene - Risk and Safety
Hazard Symbols | Xi - Irritant
|
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin.
R14 - Reacts violently with water
|
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S37/39 - Wear suitable gloves and eye/face protection
|
WGK Germany | 3 |
HS Code | 29319090 |
2-Acetoxymethyl-3-(trimethylsilyl)propene - Introduction
2-(Trimethylsilylmethyl)allyl acetate is an organic compound with the chemical formula C10H20O2Si. It is a colorless liquid with a special smell. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: colorless liquid
-Molecular weight: 200.35g/mol
-Boiling Point: 150-152°C
-Density: about 0.87 g/mL
-Melting point:-90°C
-Solubility: Soluble in organic solvents such as ethanol and dimethylformamide
Use:
- 2-(Trimethylsilylmethyl)allyl acetate is commonly used as an intermediate in organic synthesis. It has a high degree of activity and reactivity, and has a wide range of applications in the synthesis of organic compounds.
-It can be used to synthesize biologically active organic compounds, such as drugs and pesticides.
Preparation Method:
2-(Trimethylsilylmethyl)allyl acetate are generally prepared by the following steps:
1. Condensation of trimethyl (silyl) acetate and quaternary ammonium salt to form acetic acid (trimethylsilyl) methane ammonium salt.
2. reacting acetic acid (trimethylsilyl) methane ammonium salt with allyl alcohol to generate 2-(Trimethylsilylmethyl)allyl acetate.
Safety Information:
There is little safety information about the 2-(Trimethylsilylmethyl)allyl acetate, so you should be cautious when using this compound and follow laboratory safety procedures. It may have an irritating effect on the skin, eyes and respiratory tract, so appropriate safety measures such as wearing protective glasses, gloves and face masks are required. Please pay attention to a well-ventilated environment when using or handling. If taken by mistake or inhaled, seek medical help immediately.
Last Update:2024-04-09 20:49:11