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Atomfair Magnesium, bromopentyl- Pentylmagnesium Bromide, Amylmagnesium bromide C5H11BrMg

Description Magnesium, bromopentyl- (CAS No. 693-25-4) is a highly reactive Grignard reagent with the molecular formula C5H11BrMg . This organomagnesium compound, also known as Pentylmagnesium Bromide or Amylmagnesium bromide, is widely utilized in synthetic organic chemistry for nucleophilic addition reactions, carbon-carbon bond formation, and the preparation of complex organic molecules. Supplied as a solution in common solvents such as diethyl ether or THF, it is packaged under inert gas to ensure stability and prevent degradation. Ideal for researchers and industrial chemists, this reagent offers high purity and consistent performance in demanding synthetic applications. Proper handling under anhydrous conditions is essential…

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Description

Description

Magnesium, bromopentyl- (CAS No. 693-25-4) is a highly reactive Grignard reagent with the molecular formula C5H11BrMg. This organomagnesium compound, also known as Pentylmagnesium Bromide or Amylmagnesium bromide, is widely utilized in synthetic organic chemistry for nucleophilic addition reactions, carbon-carbon bond formation, and the preparation of complex organic molecules. Supplied as a solution in common solvents such as diethyl ether or THF, it is packaged under inert gas to ensure stability and prevent degradation. Ideal for researchers and industrial chemists, this reagent offers high purity and consistent performance in demanding synthetic applications. Proper handling under anhydrous conditions is essential due to its moisture-sensitive nature.

  • CAS No: 693-25-4
  • Molecular Formula: C5H11BrMg
  • Molecular Weight: 175.35
  • Exact Mass: 173.98945
  • Monoisotopic Mass: 173.98945
  • IUPAC Name: magnesium;pentane;bromide
  • SMILES: CCCC[CH2-].[Mg+2].[Br-]
  • Synonyms: 693-25-4, Magnesium, bromopentyl-, Pentylmagnesium Bromide, Amylmagnesium bromide, Bromopentylmagnesium

Application

Magnesium, bromopentyl- is primarily used as a Grignard reagent in organic synthesis for the formation of carbon-carbon bonds. It reacts with carbonyl compounds such as aldehydes, ketones, and esters to produce secondary and tertiary alcohols. This reagent is also employed in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its versatility makes it valuable for constructing complex molecular architectures in research and industrial settings.

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