Isopropylmagnesium chloride lithium chloride complex solution

1.3 M solution in THF, MkSeal

  • Product Code: 88886
  CAS:    745038-86-2
Molecular Weight: 145.24 g./mol Molecular Formula: C₃H₇Cl₂LiMg
EC Number: MDL Number: MFCD07784514
Melting Point: Boiling Point:
Density: 1.05 Storage Condition: 2~8 ℃
Product Description: Isopropylmagnesium chloride lithium chloride complex solution is widely used in organic synthesis as a Grignard reagent. It is particularly effective in the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. The solution is often employed in nucleophilic addition reactions to carbonyl compounds, such as aldehydes and ketones, to synthesize alcohols. It is also utilized in the alkylation of various organic substrates, enabling the introduction of isopropyl groups into target molecules. Its compatibility with lithium chloride enhances reactivity and stability, making it a preferred choice for complex synthetic transformations. Additionally, it is used in the preparation of organometallic compounds and as a catalyst in certain polymerization processes.
Product Specification:
Test Specification
APPEARANCE GREY TO BLACK LIQUID
ASSAYAS SEC-BUTANOL TITRATION 1.3 M
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
100.000 10-20 days $55.81
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-
500.000 10-20 days $149.71
+
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800.000 10-20 days $239.42
+
-
1000.000 10-20 days $247.52
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Isopropylmagnesium chloride lithium chloride complex solution
Isopropylmagnesium chloride lithium chloride complex solution is widely used in organic synthesis as a Grignard reagent. It is particularly effective in the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. The solution is often employed in nucleophilic addition reactions to carbonyl compounds, such as aldehydes and ketones, to synthesize alcohols. It is also utilized in the alkylation of various organic substrates, enabling the introduction of isopropyl groups into target molecules. Its compatibility with lithium chloride enhances reactivity and stability, making it a preferred choice for complex synthetic transformations. Additionally, it is used in the preparation of organometallic compounds and as a catalyst in certain polymerization processes.
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