0.5M 3-Chloro-4-Fluorophenylmagnesium Bromide in THF, AcroSeal®—high-purity Grignard reagent for halogen-metal exchange, air/moisture-sensitive, sealed for stability.
₹20,902.00 Original price was: ₹20,902.00.₹14,631.00Current price is: ₹14,631.00.
Product Name – 3-Chloro-4-Fluorophenylmagnesium Bromide, 0.5M Solution in THF, AcroSeal® Quantity/Pack Size – 50ML Form – Liquid (Solution in THF) Grade – Reagent Grade Application – Grignard reagent for organic synthesis, halogen-metal exchange
3-Chloro-4-Fluorophenylmagnesium Bromide, 0.5M Solution in THF (AcroSeal®), is a highly reactive Grignard reagent designed for precision in organic synthesis. This air- and moisture-sensitive solution is stabilized in tetrahydrofuran (THF), ensuring optimal reactivity for halogen-metal exchange reactions. The 0.5M concentration provides a balanced reactivity profile, making it suitable for synthesizing complex aromatic compounds with fluorine and chlorine substituents. The AcroSeal® packaging guarantees minimal exposure to atmospheric contaminants, preserving the reagent’s integrity until use. This reagent-grade solution is ideal for researchers requiring consistent performance in nucleophilic addition, coupling, or substitution reactions. Its sealed format minimizes handling risks while maintaining high purity, ensuring reproducible results in demanding laboratory applications. The solution’s stability in THF further enhances its versatility across a range of synthetic protocols.
When stored unopened in its original AcroSeal® packaging at 2–8°C, the solution retains stability for up to 12 months. Avoid prolonged exposure to air or moisture.
Yes, it is effective in cross-coupling reactions like Kumada or Negishi couplings, provided the reaction conditions are optimized for the fluorine and chlorine substituents.
Standard borosilicate glassware is suitable, but ensure it is dry and inert (e.g., oven-dried or flame-dried) to prevent premature decomposition of the Grignard reagent.
Alternatives include 4-fluorophenylmagnesium bromide or 3-chlorophenylmagnesium bromide, though reactivity and selectivity may vary due to the absence of the combined fluorine/chlorine substituents.
Neutralize with a dilute acid (e.g., 1M HCl) in a well-ventilated fume hood, then follow local regulations for hazardous chemical disposal. Never discard untreated reagent.
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₹20,902.00 Original price was: ₹20,902.00.₹14,631.00Current price is: ₹14,631.00.
0.5M 3-Chloro-4-Fluorophenylmagnesium Bromide in THF, AcroSeal®—high-purity Grignard reagent for halogen-metal exchange, air/moisture-sensitive, sealed for stability.
Product Name – 3-Chloro-4-Fluorophenylmagnesium Bromide, 0.5M Solution in THF, AcroSeal® Quantity/Pack Size – 50ML Form – Liquid (Solution in THF) Grade – Reagent Grade Application – Grignard reagent for organic synthesis, halogen-metal exchange
3-Chloro-4-Fluorophenylmagnesium Bromide, 0.5M Solution in THF (AcroSeal®), is a highly reactive Grignard reagent designed for precision in organic synthesis. This air- and moisture-sensitive solution is stabilized in tetrahydrofuran (THF), ensuring optimal reactivity for halogen-metal exchange reactions. The 0.5M concentration provides a balanced reactivity profile, making it suitable for synthesizing complex aromatic compounds with fluorine and chlorine substituents. The AcroSeal® packaging guarantees minimal exposure to atmospheric contaminants, preserving the reagent’s integrity until use. This reagent-grade solution is ideal for researchers requiring consistent performance in nucleophilic addition, coupling, or substitution reactions. Its sealed format minimizes handling risks while maintaining high purity, ensuring reproducible results in demanding laboratory applications. The solution’s stability in THF further enhances its versatility across a range of synthetic protocols.
When stored unopened in its original AcroSeal® packaging at 2–8°C, the solution retains stability for up to 12 months. Avoid prolonged exposure to air or moisture.
Yes, it is effective in cross-coupling reactions like Kumada or Negishi couplings, provided the reaction conditions are optimized for the fluorine and chlorine substituents.
Standard borosilicate glassware is suitable, but ensure it is dry and inert (e.g., oven-dried or flame-dried) to prevent premature decomposition of the Grignard reagent.
Alternatives include 4-fluorophenylmagnesium bromide or 3-chlorophenylmagnesium bromide, though reactivity and selectivity may vary due to the absence of the combined fluorine/chlorine substituents.
Neutralize with a dilute acid (e.g., 1M HCl) in a well-ventilated fume hood, then follow local regulations for hazardous chemical disposal. Never discard untreated reagent.
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