5-Fluoro-2-methylphenylmagnesium bromide is an organomagnesium compound, specifically a Grignard reagent, which is characterized by its reactivity and utility in organic synthesis. This compound features a phenyl ring substituted with a fluorine atom and a methyl group, indicating its potential for electrophilic aromatic substitution reactions. As a Grignard reagent, it is highly reactive towards electrophiles, allowing for the formation of carbon-carbon bonds. The presence of the bromide ion suggests that it is formed from the reaction of 5-fluoro-2-methylphenyl bromide with magnesium metal. This compound is typically handled under anhydrous conditions due to its sensitivity to moisture, which can lead to hydrolysis and the formation of unwanted byproducts. In terms of physical properties, Grignard reagents are generally colorless to pale yellow liquids or solids, depending on their structure and purity. The compound's reactivity makes it valuable in the synthesis of various organic compounds, including alcohols, ketones, and other functionalized molecules. Proper safety precautions are essential when working with this reagent due to its flammability and reactivity.

5-fluoro-2-methylphenylmagnesium bromide

186496-59-3: 5-Fluoro-2-methylphenylmagnesium bromide is an organomagnesium compound, specifically a Grignard reagent, which is characterized by its reactivity and utility in organic synthesis. This compound features a phenyl ring substituted with a fluorine atom and a methyl group, indicating its potential for electrophilic aromatic substitution reactions. As a Grignard reagent, it is highly reactive towards electrophiles, allowing for the formation of carbon-carbon bonds. The presence of the bromide ion suggests that it is formed from the reaction of 5-fluoro-2-methylphenyl bromide with magnesium metal. This compound is typically handled under anhydrous conditions due to its sensitivity to moisture, which can lead to hydrolysis and the formation of unwanted byproducts. In terms of physical properties, Grignard reagents are generally colorless to pale yellow liquids or solids, depending on their structure and purity. The compound's reactivity makes it valuable in the synthesis of various organic compounds, including alcohols, ketones, and other functionalized molecules. Proper safety precautions are essential when working with this reagent due to its flammability and reactivity.

CAS 186496-59-3

5-fluoro-2-methylphenylmagnesium bromide

5-Fluoro-2-methylphenylmagnesium bromide

Ref: 54-PC4644