Di-sec-butylmagnesium - Lithium Chloride

13% in tetrahydrofuran, about 0.8 mol/L

Reagent Code: #174933
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CAS Number 943143-06-4

science Other reagents with same CAS 943143-06-4

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Weight 180.93 g/mol
Formula C₈H₁₈Mg·LiCl
inventory_2 Storage & Handling
Storage Room temperature, stored in inert gas

description Product Description

Used as a highly reactive organometallic reagent in organic synthesis, particularly in cross-coupling reactions and nucleophilic additions. Its enhanced solubility and stability in the presence of lithium chloride make it effective for deprotonation of weakly acidic substrates and for generating carbanions in a controlled manner. Commonly employed in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals, where selective carbon-carbon bond formation is required. Also utilized in directed ortho-metalation strategies when working with aromatic systems bearing directing groups.

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inventory 10ml
10-20 days ฿2,800.00

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Di-sec-butylmagnesium - Lithium Chloride
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Used as a highly reactive organometallic reagent in organic synthesis, particularly in cross-coupling reactions and nucleophilic additions. Its enhanced solubility and stability in the presence of lithium chloride make it effective for deprotonation of weakly acidic substrates and for generating carbanions in a controlled manner. Commonly employed in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals, where selective carbon-carbon bond formation is required. Also uti

Used as a highly reactive organometallic reagent in organic synthesis, particularly in cross-coupling reactions and nucleophilic additions. Its enhanced solubility and stability in the presence of lithium chloride make it effective for deprotonation of weakly acidic substrates and for generating carbanions in a controlled manner. Commonly employed in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals, where selective carbon-carbon bond formation is required. Also utilized in directed ortho-metalation strategies when working with aromatic systems bearing directing groups.

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