sec-Butylmagnesium Chloride - Lithium Chloride

15% in tetrahydrofuran, about 1.2mol/L

  • Product Code: 94946
  CAS:    1032768-06-1
Molecular Weight: 159.26 g./mol Molecular Formula: C₄H₉ClMgLiCl
EC Number: MDL Number:
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Density: Storage Condition: room temperature, in an inert gas
Product Description: sec-Butylmagnesium Chloride - Lithium Chloride is widely used as a Grignard reagent in organic synthesis. Its primary application is in the formation of carbon-carbon bonds, making it essential for constructing complex organic molecules. It is particularly effective in alkylation reactions, where it introduces sec-butyl groups into target compounds. This reagent is also utilized in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where precise control over molecular structure is critical. Additionally, its enhanced stability, due to the presence of lithium chloride, allows for more efficient and selective reactions, especially in challenging synthetic pathways. It is often employed in industrial and laboratory settings for the production of intermediates and active ingredients in various chemical processes.
Product Specification:
Test Specification
APPEARANCE Liquid
CONCENTRATIONSEC BUTANOL METHOD 15 19%
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
10.000 10-20 days ฿2,370.00
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sec-Butylmagnesium Chloride - Lithium Chloride
sec-Butylmagnesium Chloride - Lithium Chloride is widely used as a Grignard reagent in organic synthesis. Its primary application is in the formation of carbon-carbon bonds, making it essential for constructing complex organic molecules. It is particularly effective in alkylation reactions, where it introduces sec-butyl groups into target compounds. This reagent is also utilized in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where precise control over molecular structure is critical. Additionally, its enhanced stability, due to the presence of lithium chloride, allows for more efficient and selective reactions, especially in challenging synthetic pathways. It is often employed in industrial and laboratory settings for the production of intermediates and active ingredients in various chemical processes.
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