Description

Lithium;magnesium;butane;dichloride (CAS No. 1032768-06-1) is a highly specialized organometallic compound with the molecular formula C₄H₉Cl₂LiMg. This complex, also known as 2-Butylmagnesium Chloride-Lithium Chloride or sec-Butylmagnesium Chloride – Lithium Chloride, is a valuable reagent for advanced synthetic chemistry applications. It is typically supplied as a solution in tetrahydrofuran (THF) or diethyl ether, ensuring optimal reactivity and handling. The compound is characterized by its high purity and stability under inert conditions, making it ideal for use in air- and moisture-sensitive reactions. Researchers and scientists utilize this reagent in the development of novel organic and organometallic compounds, particularly in the fields of pharmaceuticals, agrochemicals, and materials science. Proper storage under an inert atmosphere (e.g., argon or nitrogen) is recommended to maintain its integrity and performance.

Properties

• CAS Number: 1032768-06-1
• Complexity: 13.5
• IUPAC Name: lithium;magnesium;butane;dichloride
• InChI: InChI=1S/C4H9.2ClH.Li.Mg/c1-3-4-2;;;;/h3H,4H2,1-2H3;2*1H;;/q-1;;;+1;+2/p-2
• InChI Key: YMUBDNJWWYNAOA-UHFFFAOYSA-L
• Exact Mass: 158.0091758
• Molecular Formula: C4H9Cl2LiMg
• Molecular Weight: 159.3
• SMILES: [Li+].CC[CH-]C.[Mg+2].[Cl-].[Cl-]
• Monoisotopic Mass: 158.0091758
• Synonyms: 1032768-06-1, lithium;magnesium;butane;dichloride, 2-Butylmagnesium Chloride-Lithium Chloride, sec-Butylmagnesium Chloride – Lithium Chloride, SCHEMBL3400407, SCHEMBL28495855, 2-Butylmagnesium Chloride – Lithium Chloride, B4643

Application

Lithium;magnesium;butane;dichloride is widely employed as a Grignard-type reagent in organic synthesis, facilitating the formation of carbon-carbon bonds in complex molecular architectures. It is particularly useful in the preparation of secondary alcohols and ketones through nucleophilic addition reactions. Additionally, this compound serves as a precursor in the synthesis of fine chemicals and active pharmaceutical ingredients (APIs). Its compatibility with lithium chloride enhances its reactivity and selectivity in various transformations, making it a preferred choice for researchers working on stereoselective synthesis.

If you are interested or have any questions, please contact us at support@atomfair.com

Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.