Magnesium, bromo(1,1-dimethylethyl)-, Fandachem
Tert-buthylmagnesium bromide
CAS: 2259-30-5
Molecular Formula: C4H9BrMg
Magnesium, bromo(1,1-dimethylethyl)-, Fandachem - Names and Identifiers
| Name | Tert-buthylmagnesium bromide |
| Synonyms | Tert-buthylmagnesium bromide Bromo(1,1-dimethylethyl)magnesium Magnesium, bromo(1,1-dimethylethyl)- Magnesium, bromo(1,1-dimethylethyl)-, Fandachem |
| CAS | 2259-30-5 |
Magnesium, bromo(1,1-dimethylethyl)-, Fandachem - Physico-chemical Properties
| Molecular Formula | C4H9BrMg |
| Molar Mass | 161.32326 |
Magnesium, bromo(1,1-dimethylethyl)-, Fandachem - Introduction
Tert-buthylmagnesium bromide is an organic compound with the chemical formula (CH3)3CMgBr. The following is a description of the nature, use, preparation and safety information of Tert-buthylmagnesium bromide:
1. nature:
-Appearance: The Tert-buthylmagnesium bromide is a colorless to light yellow liquid.
-Solubility: It is soluble in anhydrous ether and hydrocarbon solvents, but insoluble in non-polar solvents, such as alkanes and aromatic hydrocarbons.
-Reactivity: Tert-buthylmagnesium bromide is a strong reducing agent, can react with a variety of functional groups, such as halogenated hydrocarbons, ketones, aldehydes and acids.
2. use:
-As an organic synthesis reagent: Tert-buthylmagnesium bromide are widely used in the synthesis of organic compounds, especially for important carbon-carbon coupling reactions such as hydroxylation reactions, olefin addition reactions, and the construction of carbon-carbon bonds.
-As an initiator: It can also be used as an initiator to promote the growth and crosslinking reaction of polymer chains.
3. preparation method:
-Laboratory preparation: Tert-buthylmagnesium bromide is usually prepared by reacting bromobutane with metal magnesium in anhydrous ether solvent.
4. Safety Information:
- Tert-buthylmagnesium bromide are highly irritating and corrosive. When in contact with skin or eyes, rinse with plenty of water immediately and seek medical help.
-When operating Tert-buthylmagnesium bromide, it should be done in a well-ventilated environment and wear appropriate personal protective equipment, such as protective glasses, gloves and laboratory coats. Take care to prevent it from coming into contact with moisture in the air, as it will produce flammable hydrogen.
-When storing, keep the Tert-buthylmagnesium bromide in a cool, dry, sealed container, away from fire and oxygen.
1. nature:
-Appearance: The Tert-buthylmagnesium bromide is a colorless to light yellow liquid.
-Solubility: It is soluble in anhydrous ether and hydrocarbon solvents, but insoluble in non-polar solvents, such as alkanes and aromatic hydrocarbons.
-Reactivity: Tert-buthylmagnesium bromide is a strong reducing agent, can react with a variety of functional groups, such as halogenated hydrocarbons, ketones, aldehydes and acids.
2. use:
-As an organic synthesis reagent: Tert-buthylmagnesium bromide are widely used in the synthesis of organic compounds, especially for important carbon-carbon coupling reactions such as hydroxylation reactions, olefin addition reactions, and the construction of carbon-carbon bonds.
-As an initiator: It can also be used as an initiator to promote the growth and crosslinking reaction of polymer chains.
3. preparation method:
-Laboratory preparation: Tert-buthylmagnesium bromide is usually prepared by reacting bromobutane with metal magnesium in anhydrous ether solvent.
4. Safety Information:
- Tert-buthylmagnesium bromide are highly irritating and corrosive. When in contact with skin or eyes, rinse with plenty of water immediately and seek medical help.
-When operating Tert-buthylmagnesium bromide, it should be done in a well-ventilated environment and wear appropriate personal protective equipment, such as protective glasses, gloves and laboratory coats. Take care to prevent it from coming into contact with moisture in the air, as it will produce flammable hydrogen.
-When storing, keep the Tert-buthylmagnesium bromide in a cool, dry, sealed container, away from fire and oxygen.
Last Update：2024-04-10 22:29:15
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