69393-13-1 Usage
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 potential applications in the pharmaceutical industry and research and development processes, where it may serve as a building block in the synthesis of other compounds or as an intermediate in the production of pharmaceutical drugs.
Uses
Used in Pharmaceutical Industry:
1-(1-Oxopentyl)-1H-imidazole is used as a building block for the synthesis of various pharmaceutical compounds due to its unique chemical structure and properties.
Used in Research and Development:
1-(1-Oxopentyl)-1H-imidazole is used as an intermediate in the production of pharmaceutical drugs, contributing to the development of new medications and therapies.
Used in Chemical Synthesis:
1-(1-Oxopentyl)-1H-imidazole is used as a key component in the synthesis of other complex organic compounds, potentially leading to the creation of novel molecules with specific applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 69393-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,9 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69393-13:
(7*6)+(6*9)+(5*3)+(4*9)+(3*3)+(2*1)+(1*3)=161
161 % 10 = 1
So 69393-13-1 is a valid CAS Registry Number.
69393-13-1Relevant articles and documents
One-pot conversion of a representative series of carboxylic acids to the corresponding methyl ketones
Hamilakis, Stylianos,Tsolomitis, Athanase
, p. 149 - 152 (2007/10/03)
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
Ohta, Shunsaku,Tsujimura, Atsuhiko,Okamoto, Masao
, p. 2762 - 2768 (2007/10/02)
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.
