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Atomfair Magnesium, chloro(1-methylpropyl)- sec-Butylmagnesium chloride C4H9ClMg

Description Magnesium, chloro(1-methylpropyl)- (CAS No. 15366-08-2) is a highly reactive organomagnesium compound with the molecular formula C4H9ClMg . Also known as sec-Butylmagnesium chloride , this Grignard reagent is widely utilized in synthetic organic chemistry for nucleophilic addition reactions, coupling processes, and the formation of carbon-carbon bonds. Supplied as a solution in common solvents such as diethyl ether or tetrahydrofuran (THF), it is moisture-sensitive and requires handling under inert conditions (e.g., nitrogen or argon atmosphere). Ideal for researchers and industrial chemists, this compound is rigorously tested for purity and reactivity to ensure consistent performance in complex synthetic applications.

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Description

Description

Magnesium, chloro(1-methylpropyl)- (CAS No. 15366-08-2) is a highly reactive organomagnesium compound with the molecular formula C4H9ClMg. Also known as sec-Butylmagnesium chloride, this Grignard reagent is widely utilized in synthetic organic chemistry for nucleophilic addition reactions, coupling processes, and the formation of carbon-carbon bonds. Supplied as a solution in common solvents such as diethyl ether or tetrahydrofuran (THF), it is moisture-sensitive and requires handling under inert conditions (e.g., nitrogen or argon atmosphere). Ideal for researchers and industrial chemists, this compound is rigorously tested for purity and reactivity to ensure consistent performance in complex synthetic applications.

  • CAS No: 15366-08-2
  • Molecular Formula: C4H9ClMg
  • Molecular Weight: 116.87
  • Exact Mass: 116.0243197
  • Monoisotopic Mass: 116.0243197
  • IUPAC Name: magnesium;butane;chloride
  • SMILES: CC[CH-]C.[Mg+2].[Cl-]
  • Synonyms: sec-Butylmagnesium chloride, 15366-08-2, Magnesium, chloro(1-methylpropyl)-, Chloro(1-methylpropyl)magnesium, EINECS 239-403-3

Application

Magnesium, chloro(1-methylpropyl)- is primarily used as a Grignard reagent in organic synthesis for the formation of carbon-carbon bonds. It is employed in nucleophilic addition reactions to carbonyl compounds, such as ketones and aldehydes, to produce secondary and tertiary alcohols. Additionally, it serves as a key intermediate in pharmaceutical and fine chemical manufacturing. Its reactivity makes it suitable for metallation and halogen-magnesium exchange reactions.

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