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Molecular Formula: C2H3BrMg
Appearance: Transparent light brown to brown solution
Molecular Weight: 131.26
Density: 0.981 g/mL at 25 °C
Flash Point: 1 °F
Storage Conditions: Refrigerator
Solubility: Readily reacts with water, carbon dioxide, alcohols, aldehydes, ketones, esters, amines, and epoxides
Concentration: 1.0 M in THF
Package Information: 100g, 500g, 1kg or customized
Vinylmagnesium bromide solution exhibits outstanding nucleophilic addition properties, selectively adding to carbonyl compounds to generate allyl alcohols, making it an excellent reagent for constructing carbon-carbon bonds.
Compared to other vinyl metal reagents, it has a wider reaction temperature window, suitable for room temperature and low temperature conditions, which helps to avoid side reactions.
C2H3BrMg is a crucial vinyl source in organic synthesis, widely used in laboratory research and industrial production, including the synthesis of pharmaceutical active molecules, polymer monomers, and functional chemicals.
Suitable for continuous reactions in scientific research, medicine, and industry, and performs well in scenarios with strict requirements for stability and metal impurities.
C2H3BrMg can be used as a pharmaceutical intermediate to construct conjugated structures or addition skeletons, and is a common grammatical tool reagent in the drug raw material route.
It is mainly used as a strong nucleophile and vinylizing agent, and is widely used in the synthesis of pharmaceutical intermediates and fine chemicals.
This compound can be used to synthesize specific monomers or polymer initiators/chain transfer agents to prepare polymer materials with specific structures and properties.
Vinylmagnesium bromide solution is used as a model compound or starting material to synthesize other complex molecules and is widely applied in research fields such as catalysis chemistry and materials science.
Vinylmagnesium bromide solution reacts violently, even explosively, with water. All operations must be performed under strictly anhydrous conditions and protected with nitrogen or argon gas.
All containers must be completely dry, otherwise the solution will decompose, affecting the reaction yield and reproducibility.
If it gets on your skin, rinse immediately with plenty of water and remove any contaminated clothing. If it gets into your eyes, rinse continuously for at least 15 minutes and seek medical attention.
C2H3BrMg reacts violently with oxidants, posing a risk of combustion or explosion, and should therefore be kept away from oxidizing substances.
When adding it to a reaction vessel or flask, it should be added slowly dropwise to avoid local temperature rise that could lead to side reactions.
1. What are the main uses of vinylmagnesium bromide solution?
It is primarily used as a Grignard reagent in organic synthesis as a vinylizing agent and nucleophile, and is widely used for carbon-carbon bond formation.
2. Can it be used directly for scale-up experiments?
Yes, but the feeding rate, temperature, and moisture content must be strictly controlled, and a small-scale test must be conducted beforehand to confirm the heat release of the reaction.
3. What is the difference between diethyl ether solution and THF solution?
Diethyl ether system is more volatile and suitable for low-boiling systems; THF has better stability and is suitable for a wider temperature range, and can be selected according to process requirements.
We are a professional Vinylmagnesium Bromide Solution supplier. For more information or to purchase Vinylmagnesium Bromide Solution(C2H3BrMg), please feel free to contact us via jomin@wolfabio.com.
Molecular Formula: C2H3BrMg
Appearance: Transparent light brown to brown solution
Molecular Weight: 131.26
Density: 0.981 g/mL at 25 °C
Flash Point: 1 °F
Storage Conditions: Refrigerator
Solubility: Readily reacts with water, carbon dioxide, alcohols, aldehydes, ketones, esters, amines, and epoxides
Concentration: 1.0 M in THF
Package Information: 100g, 500g, 1kg or customized
Vinylmagnesium bromide solution exhibits outstanding nucleophilic addition properties, selectively adding to carbonyl compounds to generate allyl alcohols, making it an excellent reagent for constructing carbon-carbon bonds.
Compared to other vinyl metal reagents, it has a wider reaction temperature window, suitable for room temperature and low temperature conditions, which helps to avoid side reactions.
C2H3BrMg is a crucial vinyl source in organic synthesis, widely used in laboratory research and industrial production, including the synthesis of pharmaceutical active molecules, polymer monomers, and functional chemicals.
Suitable for continuous reactions in scientific research, medicine, and industry, and performs well in scenarios with strict requirements for stability and metal impurities.
C2H3BrMg can be used as a pharmaceutical intermediate to construct conjugated structures or addition skeletons, and is a common grammatical tool reagent in the drug raw material route.
It is mainly used as a strong nucleophile and vinylizing agent, and is widely used in the synthesis of pharmaceutical intermediates and fine chemicals.
This compound can be used to synthesize specific monomers or polymer initiators/chain transfer agents to prepare polymer materials with specific structures and properties.
Vinylmagnesium bromide solution is used as a model compound or starting material to synthesize other complex molecules and is widely applied in research fields such as catalysis chemistry and materials science.
Vinylmagnesium bromide solution reacts violently, even explosively, with water. All operations must be performed under strictly anhydrous conditions and protected with nitrogen or argon gas.
All containers must be completely dry, otherwise the solution will decompose, affecting the reaction yield and reproducibility.
If it gets on your skin, rinse immediately with plenty of water and remove any contaminated clothing. If it gets into your eyes, rinse continuously for at least 15 minutes and seek medical attention.
C2H3BrMg reacts violently with oxidants, posing a risk of combustion or explosion, and should therefore be kept away from oxidizing substances.
When adding it to a reaction vessel or flask, it should be added slowly dropwise to avoid local temperature rise that could lead to side reactions.
1. What are the main uses of vinylmagnesium bromide solution?
It is primarily used as a Grignard reagent in organic synthesis as a vinylizing agent and nucleophile, and is widely used for carbon-carbon bond formation.
2. Can it be used directly for scale-up experiments?
Yes, but the feeding rate, temperature, and moisture content must be strictly controlled, and a small-scale test must be conducted beforehand to confirm the heat release of the reaction.
3. What is the difference between diethyl ether solution and THF solution?
Diethyl ether system is more volatile and suitable for low-boiling systems; THF has better stability and is suitable for a wider temperature range, and can be selected according to process requirements.
We are a professional Vinylmagnesium Bromide Solution supplier. For more information or to purchase Vinylmagnesium Bromide Solution(C2H3BrMg), please feel free to contact us via jomin@wolfabio.com.
