69393-13-1

Basic information

• Product Name: 1-(1-Oxopentyl)-1H-imidazole
• Synonyms: 1-(1-Oxopentyl)-1H-imidazole
• CAS NO: 69393-13-1
• Molecular Formula: C₈H₁₂N₂O
• Molecular Weight: 0
• Mol File: 69393-13-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(1-Oxopentyl)-1H-imidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(1-Oxopentyl)-1H-imidazole(69393-13-1)
• EPA Substance Registry System: 1-(1-Oxopentyl)-1H-imidazole(69393-13-1)

Safety Data

• Hazardous Substances Data: 69393-13-1(Hazardous Substances Data)

Usage

General Description

1-(1-Oxopentyl)-1H-imidazole is a chemical compound with the molecular formula C7H10N2O. It is a derivative of imidazole and contains a pentyl ketone group. 1-(1-Oxopentyl)-1H-imidazole has various potential applications in pharmaceuticals, as well as in research and development processes. It may have uses as a building block in the synthesis of other compounds, or as an intermediate in the production of pharmaceutical drugs. The specific properties and potential uses of 1-(1-Oxopentyl)-1H-imidazole may be further explored through chemical analysis and experimentation.

Upstream product

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Downstream Products

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• 80601-67-8 1-cyclohexylheptane-1,3-dione 
• 40568-55-6 1-(phenyl)-1,3-heptanedione 

Relevant articles and documents

One-pot conversion of a representative series of carboxylic acids to the corresponding methyl ketones

The use of imidazolide activation method for direct acylation of Meldrum's acid with carboxylic acids, and the subsequent acidic hydrolysis of the acylated products to methyl ketones, provide a simple and efficient method for a one-pot conversion of carboxylic acids to the corresponding methyl ketones.

Use of β-Ketocarboxylic Acids for Syntheses of 6-Substituted 4-Hydroxy-2-pyrones and Acyclic β-Diketones

β-Ketocarboxylic acids including β-ketoglutaric acid half-esters were cyclized by treating them with 1,1'-carbonyl-diimidazole to give 6-substituted 3-acyl-4-hydroxy-2-pyrones in good yields. 5-Aryl-3,5-dioxo-1-pentanoic acid and monomethyl malonate gave 6-aryl-4-hydroxy-2-pyrone and dimethyl β-ketoglutarate, respectively, on similar treatment.Anibin, one of the Aniba alkaloids, was synthesized from 5-(3-pyridyl)-4-hydroxy-2-pyrone.In addition, it was confirmed that reaction of magnesium β-ketocarboxylate with acylimidazolide gave the corresponding acyclic β-diketone in excellent yield.Keywords - β-ketocarboxilic acid; biogenetic-type synthesis; 4-hydroxy-2-pyrone; β-polyketide; β-ketoglutaric acid; dehydroacetic acid; anibin; Aniba alkaloid; 3-acyl-4-hydroxy-2-pyrone; β-diketone.