77542-18-8

Basic information

• Product Name: PiperidiniuM, 1-ethyl-1-Methyl-4-oxo-, iodide (1:1)
• Synonyms: PiperidiniuM, 1-ethyl-1-Methyl-4-oxo-, iodide (1:1);PiperidiniuM, 1-ethyl-1-Methyl-4-oxo-, iodide;1-Ethyl-1-methyl-4-oxo-piperidinium iodide;EOS-60490;1-ethyl-1-methylpiperidin-1-ium-4-one,iodide
• CAS NO: 77542-18-8
• Molecular Formula: C₈H₁₆NO*I
• Molecular Weight: 269.12321
• Mol File: 77542-18-8.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• CAS DataBase Reference: PiperidiniuM, 1-ethyl-1-Methyl-4-oxo-, iodide (1:1)(CAS DataBase Reference)
• NIST Chemistry Reference: PiperidiniuM, 1-ethyl-1-Methyl-4-oxo-, iodide (1:1)(77542-18-8)
• EPA Substance Registry System: PiperidiniuM, 1-ethyl-1-Methyl-4-oxo-, iodide (1:1)(77542-18-8)

Safety Data

• Hazardous Substances Data: 77542-18-8(Hazardous Substances Data)

Usage

Description

PiperidiniuM, 1-ethyl-1-Methyl-4-oxo-, iodide (1:1) is a quaternary ammonium salt with the molecular formula C8H16INO, typically appearing as a white or off-white crystalline solid. It is a versatile chemical compound commonly used in organic synthesis and medicinal chemistry.

Uses

Used in Organic Synthesis:
PiperidiniuM, 1-ethyl-1-Methyl-4-oxo-, iodide (1:1) is used as a reagent in the synthesis of various pharmaceuticals and organic compounds, contributing to the creation of a wide range of chemical products.
Used in Medicinal Chemistry:
PiperidiniuM, 1-ethyl-1-Methyl-4-oxo-, iodide (1:1) is utilized in the development of new medications due to its potential antifungal and antibacterial properties, making it a valuable asset in the fight against infections.
Used in Antifungal Applications:
PiperidiniuM, 1-ethyl-1-Methyl-4-oxo-, iodide (1:1) is employed as an antifungal agent, helping to combat fungal infections by inhibiting the growth and proliferation of fungi.
Used in Antibacterial Applications:
It is also used as an antibacterial agent, working to prevent the growth of bacteria and treat bacterial infections.
Used in Anti-Inflammatory Research:
PiperidiniuM, 1-ethyl-1-Methyl-4-oxo-, iodide (1:1) has been studied for its potential as an anti-inflammatory agent, which could be beneficial in the treatment of various inflammatory conditions.
Used in Neurological Disorder Treatment:
PiperidiniuM, 1-ethyl-1-Methyl-4-oxo-, iodide (1:1) is being investigated for its potential use in the treatment of neurological disorders, offering hope for new therapeutic approaches to manage such conditions.

Downstream Products

• 228246-75-1 (R)-1-(acenaphthen-1-yl)-piperidine-4-one 
• 228246-76-2 (S)-1-(acenaphthen-1-yl)-piperidine-4-one 
• 252285-20-4 cis-1-(4-isopropylcyclohexyl)piperidin-4-one 
• 494863-58-0 trans-1-(4-isopropylcyclohexyl)piperidin-4-one 
• 709024-86-2 1-dicyclohexylmethyl-piperidin-4-one 
• 901779-56-4 trans-1-(4-tert-butylcyclohexyl)-4-piperidone 
• 901779-55-3 cis-1-(4-tert-butylcyclohexyl)-4-piperidone 
• 901779-52-0 trans-1-(4-ethylcyclohexyl)-4-piperidone 
• 901779-51-9 cis-1-(4-ethylcyclohexyl)-4-piperidone 
• 901779-54-2 trans-1-(4-n-propylcyclohexyl)-4-piperidone 
• 901779-53-1 cis-1-(4-n-propylcyclohexyl)-4-piperidone 
• 901779-50-8 trans-1-(4-methylcyclohexyl)-4-piperidone 
• 901779-49-5 cis-1-(4-methylcyclohexyl)-4-piperidone 
• 950772-08-4 1-[trans-4-(ethyloxy)cyclohexyl]-4-piperidinone 

Relevant articles and documents

Ionic liquids that form adducts with alcohols

A class of ionic liquids with a built-in active ketone functionality is shown to form adducts with structurally diverse alcohols. The positions of the equilibria for adduct formation are shown to be dependent on the structure of the alcohols. How these functionalised ionic liquids could be applied in altering vapour phase compositions of alcohols and in separations of perfumery alcohols are demonstrated, here.