trimethoxy(η5-2,4-cyclopentadien-1-yl)titanium
trimethoxy(η5-2,4-cyclopentadien-1-yl)titanium
CAS: 12145-64-1
Molecular Formula: C8H9O3Ti
trimethoxy(η5-2,4-cyclopentadien-1-yl)titanium - Names and Identifiers
| Name | trimethoxy(η5-2,4-cyclopentadien-1-yl)titanium |
| Synonyms | trimethoxy(η5-2,4-cycL trimethoxy(η5-2,4-cyclopentadien-1-yl)titanium |
| CAS | 12145-64-1 |
trimethoxy(η5-2,4-cyclopentadien-1-yl)titanium - Physico-chemical Properties
| Molecular Formula | C8H9O3Ti |
| Molar Mass | 201.02 |
trimethoxy(η5-2,4-cyclopentadien-1-yl)titanium - Introduction
trimethoxy(η5-2,4-cyclopentadien-1-yl)titanium is an organometallic compound with the chemical formula (C5H5)Ti(OCOMe)3. It is a powdery solid that does not volatilize at room temperature. The compound is soluble in organic solvents such as ethanol and dimethylformamide.
trimethoxy(η5-2,4-cyclopentadien-1-yl)titanium have a variety of applications. It is an important organic synthesis reagent and is often used to catalyze asymmetric synthesis reactions. It can be used as a transition metal catalyst to participate in various organic reactions, such as hydrogenation, siliconization, boric acid esterification and other reactions. In addition, it can also be used as a precursor for the synthesis of metal-containing organic compounds, or as a protecting group for organic molecules.
The method for preparing trimethoxy(η5-2,4-cyclopentadien-1-yl)titanium usually uses coordination chemistry technology. A common preparation method is to react cyclopentadienyl lithium with trimethoxysilane to form trimethoxycyclopentadienyl silane, which is then reacted with dichlorodimethyltitanium to obtain the target product.
with regard to safety information, trimethoxy(η5-2,4-cyclopentadien-1-yl)titanium is relatively stable under normal operating conditions, but because it is an organometallic compound and has certain toxicity, it is necessary to follow the corresponding safety operation procedures during operation. Personal protective equipment such as goggles, gloves and laboratory suits should be worn when in use. In addition, avoid contact with moisture and oxygen in the air, as it may decompose or hydrolyze under moisture. If desired, it is possible to operate under an inert atmosphere.
trimethoxy(η5-2,4-cyclopentadien-1-yl)titanium have a variety of applications. It is an important organic synthesis reagent and is often used to catalyze asymmetric synthesis reactions. It can be used as a transition metal catalyst to participate in various organic reactions, such as hydrogenation, siliconization, boric acid esterification and other reactions. In addition, it can also be used as a precursor for the synthesis of metal-containing organic compounds, or as a protecting group for organic molecules.
The method for preparing trimethoxy(η5-2,4-cyclopentadien-1-yl)titanium usually uses coordination chemistry technology. A common preparation method is to react cyclopentadienyl lithium with trimethoxysilane to form trimethoxycyclopentadienyl silane, which is then reacted with dichlorodimethyltitanium to obtain the target product.
with regard to safety information, trimethoxy(η5-2,4-cyclopentadien-1-yl)titanium is relatively stable under normal operating conditions, but because it is an organometallic compound and has certain toxicity, it is necessary to follow the corresponding safety operation procedures during operation. Personal protective equipment such as goggles, gloves and laboratory suits should be worn when in use. In addition, avoid contact with moisture and oxygen in the air, as it may decompose or hydrolyze under moisture. If desired, it is possible to operate under an inert atmosphere.
Last Update：2024-04-10 22:29:15
