134560-43-3

Basic information

• Product Name: Cyclohexaneacetamide, N-methoxy-N-methyl-
• CAS NO: 134560-43-3
• Molecular Formula: C10H19NO2
• Molecular Weight: 185.266
• Mol File: 134560-43-3.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Cyclohexaneacetamide, N-methoxy-N-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexaneacetamide, N-methoxy-N-methyl-(134560-43-3)
• EPA Substance Registry System: Cyclohexaneacetamide, N-methoxy-N-methyl-(134560-43-3)

Safety Data

• Hazardous Substances Data: 134560-43-3(Hazardous Substances Data)

Upstream product

• 5292-21-7 Cyclohexylacetic acid 
• 1117-97-1 N,0-dimethylhydroxylamine 
• 6638-79-5 N,O-dimethylhydroxylamine*hydrochloride 
• 23860-35-7 cyclohexylacetic acid chloride 

Downstream Products

• 149108-75-8 2-cyclohexyl-1-(pyridin-2-yl)ethan-1-one 
• 1414926-65-0 2-cyclohexyl-1-(2-hydroxyphenyl)ethan-1-one 
• 1414926-66-1 methyl 4-(2-(2-cyclohexylacetyl)phenoxy)-3-nitrobenzoate 
• 1414926-67-2 4-[1-cyclohexyl-2-(2-hydroxy-phenyl)-2-oxo-ethyl]-3-nitrobenzoic acid methyl ester 
• 863578-50-1 3-cyclohexyl-2-(2-hydroxy-phenyl)-1H-indole-6-carboxylic acid methyl ester 
• 1281318-51-1 2-cyclohexyl-1-(2-methoxyphenyl)ethan-1-one 
• 103-78-6 4-cyclohexyl-butan-2-one 
• 134560-44-4 2-Cyclohexyl-1-[4-(2-Dioxolanyl)Phenyl]Ethanone 
• 149108-78-1 (R)-2-((S)-2-Cyclohexyl-1-pyridin-2-yl-ethylamino)-2-phenyl-ethanol 
• 183962-51-8 1-(S,R)-(pyridin-2-yl)-2-cyclohexylethylamine 

Relevant articles and documents

Metal complex, electroluminescent device containing metal complex and application of metal complex

The invention provides a metal complex, an electroluminescent device containing the metal complex and application of the electroluminescent device, the metal complex has an M(La)m(Lb)n structure, the metal complex provided by the invention can more effectively finely adjust the luminescence color and adjust the luminescence peak width, so that the half-peak width is narrowed, the luminescence color is more saturated, the device efficiency is improved, and the current efficiency and the external quantum efficiency are relatively high.

'Wake-Up Call of A Sleeping Beauty': Straightforward Synthesis of Functionalized β-(2-Pyridyl) Ketones from 2,6-Lutidine

β-(2-Pyridyl) ketones are a unique class of heterocycles with valuable physicochemical properties and emerging relevance as pharmacophores. Herein we report a one-step process for the preparation of various substituted β-(2-pyridyl) ketones from the common starting material, 2,6-lutidine. Furthermore, we demonstrate the utility of this building block by synthesizing of a small set of antimalarial natural products.

A Weinreb amide approach to the synthesis of trifluoromethylketones

A novel route to access trifluoromethylketones (TFMKs) from Weinreb amides is reported. This represents the first documented case of the Ruppert-Prakash reagent (TMS-CF3) reacting in a constructive manner with an amide and enables synthesis of TMFKs without risk of over-trifluoromethylation.