TERT-BUTYLDIMETHYL(2-PROPYNYLOXY)SILANE
tert-butyl(dimethyl)(prop-2-yn-1-yloxy)silane
CAS: 76782-82-6
Molecular Formula: C9H18OSi
TERT-BUTYLDIMETHYL(2-PROPYNYLOXY)SILANE - Names and Identifiers
TERT-BUTYLDIMETHYL(2-PROPYNYLOXY)SILANE - Physico-chemical Properties
| Molecular Formula | C9H18OSi |
| Molar Mass | 170.32 |
| Density | 0.84 g/mL at 25 °C (lit.) |
| Boling Point | 40 °C/8 mmHg (lit.) |
| Flash Point | 108°F |
| Solubility | Diethyl Ether, Ethyl Acetate, Hexane |
| Vapor Presure | 3.51mmHg at 25°C |
| Appearance | Oil |
| Specific Gravity | 0.84 |
| Color | Colorless |
| Sensitive | 7: reacts slowly with moisture/water |
| Refractive Index | n20/D 1.429(lit.) |
TERT-BUTYLDIMETHYL(2-PROPYNYLOXY)SILANE - Risk and Safety
| Risk Codes | 10 - Flammable |
| Safety Description | 16 - Keep away from sources of ignition. |
| UN IDs | UN 1993 3/PG 3 |
| WGK Germany | 3 |
TERT-BUTYLDIMETHYL(2-PROPYNYLOXY)SILANE - Introduction
tert-butyl(dimethyl)(prop-2-yn-1-yloxy)silane is an organosilicon compound with the chemical formula C9H18OSi, which contains one propargyloxy group and one tert-butyl group in the molecule. The following is a description of the properties, uses, preparation and safety information of the compound:
1. nature:
-Appearance: colorless transparent liquid
-Molecular weight: 170.32g/mol
-Boiling Point: 85-87°C
-Density: 0.80 g/mL
-Solubility: Soluble in non-polar solvents such as benzene and ether
2. use:
-As an organic silicon compound, it is often used to synthesize functional materials;
-can be used as a reagent in organic synthesis, such as a reagent for oxidation, reduction and substitution reactions;
-In chemical research, it can be used as an intermediate in organic synthesis reactions.
3. preparation method:
- tert-butyl(dimethyl)(prop-2-yn-1-yloxy)silane can be prepared by chemical synthesis, the specific steps are as follows:
-Step 1: Use the malodorous gas as the solvent, and introduce the gas into the reactor through the pipeline;
-Step 2: A Zhan-blown acid treatment agent generates silver ions from silver compounds, and in the presence of silver ions, an acid-catalyzed acetylenic silver addition reaction occurs with acetylenic alcohols to generate acetylenic hydrocarbons;
-step 3: catalytically adding the alkyne obtained in step 2 to tert-butanol to generate propargyl alcohol;
-Step 4: Use aluminum-lithium alloy to reduce propargyl alcohol to propargyl hydrocarbon;
-Step 5: React propargyl with dimethylchlorosilane through silicon chemical reaction to obtain the final product tert-butyl(dimethyl)(prop-2-yn-1-yloxy)silane.
4. Safety Information:
- tert-butyl(dimethyl)(prop-2-yn-1-yloxy)silane is relatively stable and is not prone to fire or explosion under normal use conditions.
-but it may be irritating and corrosive to the eyes and skin, use should wear personal protective equipment, such as glasses and gloves.
-Avoid inhaling its vapors or contacting its liquids to avoid discomfort or damage to health.
-In use or storage, should comply with the relevant safety guidelines and regulations.
Please note that the above information is for reference only. Please follow safe operations when using the compound and refer to the exact chemical substance safety data sheet (MSDS).
1. nature:
-Appearance: colorless transparent liquid
-Molecular weight: 170.32g/mol
-Boiling Point: 85-87°C
-Density: 0.80 g/mL
-Solubility: Soluble in non-polar solvents such as benzene and ether
2. use:
-As an organic silicon compound, it is often used to synthesize functional materials;
-can be used as a reagent in organic synthesis, such as a reagent for oxidation, reduction and substitution reactions;
-In chemical research, it can be used as an intermediate in organic synthesis reactions.
3. preparation method:
- tert-butyl(dimethyl)(prop-2-yn-1-yloxy)silane can be prepared by chemical synthesis, the specific steps are as follows:
-Step 1: Use the malodorous gas as the solvent, and introduce the gas into the reactor through the pipeline;
-Step 2: A Zhan-blown acid treatment agent generates silver ions from silver compounds, and in the presence of silver ions, an acid-catalyzed acetylenic silver addition reaction occurs with acetylenic alcohols to generate acetylenic hydrocarbons;
-step 3: catalytically adding the alkyne obtained in step 2 to tert-butanol to generate propargyl alcohol;
-Step 4: Use aluminum-lithium alloy to reduce propargyl alcohol to propargyl hydrocarbon;
-Step 5: React propargyl with dimethylchlorosilane through silicon chemical reaction to obtain the final product tert-butyl(dimethyl)(prop-2-yn-1-yloxy)silane.
4. Safety Information:
- tert-butyl(dimethyl)(prop-2-yn-1-yloxy)silane is relatively stable and is not prone to fire or explosion under normal use conditions.
-but it may be irritating and corrosive to the eyes and skin, use should wear personal protective equipment, such as glasses and gloves.
-Avoid inhaling its vapors or contacting its liquids to avoid discomfort or damage to health.
-In use or storage, should comply with the relevant safety guidelines and regulations.
Please note that the above information is for reference only. Please follow safe operations when using the compound and refer to the exact chemical substance safety data sheet (MSDS).
Last Update：2024-04-10 22:29:15
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View History
TERT-BUTYLDIMETHYL(2-PROPYNYLOXY)SILANE
反式-3-氯-2-丙烯基羟胺
乙二胺四乙酸镁二钠盐水合物
3',4'-(二辛氧荃)苯甲醛
Α-氨基环己基乙酸
C.I. Direct Blue 53, tetrasodium salt (8CI)
反式-3-氯-2-丙烯基羟胺
乙二胺四乙酸镁二钠盐水合物
3',4'-(二辛氧荃)苯甲醛
Α-氨基环己基乙酸
C.I. Direct Blue 53, tetrasodium salt (8CI)