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

General Description

PiperidiniuM, 1-ethyl-1-Methyl-4-oxo-, iodide (1:1) is a chemical compound that is commonly used in organic synthesis and medicinal chemistry. It is a quaternary ammonium salt with the molecular formula C8H16INO, and it is typically a white or off-white crystalline solid. PiperidiniuM, 1-ethyl-1-Methyl-4-oxo-, iodide (1:1) is often used as a reagent in the synthesis of various pharmaceuticals and organic compounds, and it is also known for its potential antifungal and antibacterial properties. Additionally, it has been studied for its potential use as an anti-inflammatory agent and in the treatment of neurological disorders. Overall, PiperidiniuM, 1-ethyl-1-Methyl-4-oxo-, iodide (1:1) is a versatile chemical with a range of potential applications in organic synthesis and medicine.

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 
• 690273-85-9 1-(2-phenylpropan-2-yl)piperidin-4-one 
• 1258304-95-8 methyl 1-(4-oxopiperidin-1-yl)cyclohexanecarboxylate 
• 610323-32-5 W-212393 
• 1238893-54-3 2-(2-(1-((R)-acenaphthen-1-yl)piperidin-4-ylamino)phenylamino)-N-methylacetamide 
• 1441792-39-7 C₁₅H₂₆N₂O₃ 
• 1441792-54-6 C₂₇H₃₂Cl₃N₃O₂ 
• 1441785-10-9 2-chloro-N-((1R)-1-(2,4-dichIorophenyl)ethyl)-5-(1-((3S)-3-piperidyl)-3,6-dihydro-2H-pyridin-4-yl)aniline 
• 1441792-49-9 (S)-t-butyl 3-(4-(4-chloro-3-((R)-1-(2,4-dichlorophenyl)ethylamino)phenyl)-5,6-dihydropyridin-1(2H)-yl)piperidine-1-carboxylate 
• 1134198-16-5 1-{trans-1-methyl-4-[(1-methylethyl)oxy]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.