4-trifluoromethyl-phenylmagnesium bromide, 1.0 M solution in Diethyl ether, Fandachem
(4-Trifluoromethylphenyl)magnesium bromide
CAS: 402-51-7
Molecular Formula: C7H4BrF3Mg
4-trifluoromethyl-phenylmagnesium bromide, 1.0 M solution in Diethyl ether, Fandachem - Names and Identifiers
4-trifluoromethyl-phenylmagnesium bromide, 1.0 M solution in Diethyl ether, Fandachem - Physico-chemical Properties
| Molecular Formula | C7H4BrF3Mg |
| Molar Mass | 249.3108696 |
| Boling Point | 156.5°C |
4-trifluoromethyl-phenylmagnesium bromide, 1.0 M solution in Diethyl ether, Fandachem - Introduction
(4-Trifluoromethylphenyl)magnesium bromide is an organic compound with the chemical formula C7H4BrF3Mg. It is usually present in the form of an organic synthesis reagent, with the crystalline form of a colorless or pale yellow solid.
The following is a description of the properties, uses, preparation methods and safety information of the compound:
Nature:
1. (4-Trifluoromethylphenyl)magnesium bromide is an organometallic compound with a strong magnesium-halogen bond.
2. It is a polar compound and is stable under inert gas atmosphere.
3. it can be substituted with other compounds, such as electrophilic substitution reaction.
4. The compound will decompose under humid conditions.
Use:
1. (4-Trifluoromethylphenyl)magnesium bromide is an important organic synthesis reagent, which can be used to synthesize other organic compounds.
2. It can be used to synthesize phenyl magnesium bromide, thereby participating in more complex chemical reactions.
Preparation Method:
Preparation of (4-Trifluoromethylphenyl) The magnesium bromide can be obtained by reacting 4-trifluoromethylbromobenzene with magnesium powder. The reaction conditions are generally under an inert gas atmosphere at room temperature to low temperature.
Safety Information:
1. This compound is sensitive to moisture and should be treated under dry and anhydrous conditions to prevent decomposition.
2. During operation, you need to pay attention to avoid skin contact and inhalation. Suitable protective equipment such as gloves, safety glasses and laboratory coats should be worn.
3. should be away from fire and high temperature objects, stored in a cool and dry place.
4. When handling the compound, safe operating procedures should be followed, and it should be operated in a well-ventilated place.
5. In the process, avoid contact with oxygen, water and moisture to prevent unnecessary reactions.
The following is a description of the properties, uses, preparation methods and safety information of the compound:
Nature:
1. (4-Trifluoromethylphenyl)magnesium bromide is an organometallic compound with a strong magnesium-halogen bond.
2. It is a polar compound and is stable under inert gas atmosphere.
3. it can be substituted with other compounds, such as electrophilic substitution reaction.
4. The compound will decompose under humid conditions.
Use:
1. (4-Trifluoromethylphenyl)magnesium bromide is an important organic synthesis reagent, which can be used to synthesize other organic compounds.
2. It can be used to synthesize phenyl magnesium bromide, thereby participating in more complex chemical reactions.
Preparation Method:
Preparation of (4-Trifluoromethylphenyl) The magnesium bromide can be obtained by reacting 4-trifluoromethylbromobenzene with magnesium powder. The reaction conditions are generally under an inert gas atmosphere at room temperature to low temperature.
Safety Information:
1. This compound is sensitive to moisture and should be treated under dry and anhydrous conditions to prevent decomposition.
2. During operation, you need to pay attention to avoid skin contact and inhalation. Suitable protective equipment such as gloves, safety glasses and laboratory coats should be worn.
3. should be away from fire and high temperature objects, stored in a cool and dry place.
4. When handling the compound, safe operating procedures should be followed, and it should be operated in a well-ventilated place.
5. In the process, avoid contact with oxygen, water and moisture to prevent unnecessary reactions.
Last Update：2024-04-10 22:29:15
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