4664-70-4

Usage

Uses

Used in Pharmaceutical Industry:
Cyclohexyl[4-(dimethylamino)phenyl]methanone serves as a crucial intermediate in the synthesis of pharmaceuticals. Its unique structure allows it to be a building block for the development of various bioactive compounds, contributing to the creation of new medications.
Used in Agrochemical Industry:
cyclohexyl[4-(dimethylamino)phenyl]methanone also plays a significant role in the agrochemical sector, where it is utilized in the preparation of agrochemicals. Its properties make it a valuable component in the development of products designed to enhance crop protection and yield.
Used in Dye and Pigment Production:
Cyclohexyl[4-(dimethylamino)phenyl]methanone is employed as a key intermediate in the production of dyes and pigments. Its chemical structure provides a foundation for creating a wide range of colors and hues used in various industries, including textiles, plastics, and printing.
Used in Specialty Chemicals:
Beyond its applications in pharmaceuticals, agrochemicals, dyes, and pigments, cyclohexyl[4-(dimethylamino)phenyl]methanone is also used as a building block in the synthesis of other specialty chemicals. Its versatility makes it a valuable asset in the chemical industry.
Used in Research and Development:
cyclohexyl[4-(dimethylamino)phenyl]methanone has been studied for its potential pharmacological properties, such as its possible use as an analgesic and anti-inflammatory agent. This makes it an important subject of research and development in the field of medicine and pharmaceuticals, as it may lead to the discovery of new therapeutic agents.

Upstream product

• 60718-41-4 Se-phenyl cyclohexanecarboselenoate 
• 121-69-7 N,N-dimethyl-aniline 
• 2719-27-9 cyclohexanylcarbonyl chloride 
• 4755-50-4 4-(dimethylamino)benzoyl chloride 
• 98-89-5 Cyclohexanecarboxylic acid 
• 126812-30-4 1,3-dioxoisoindolin-2-yl cyclohexanecarboxylate 
• 28075-50-5 cyclohex-1-en-1-yl trifluoromethane sulfonate 
• 100-10-7 4-dimethylamino-benzaldehyde 
• 68571-10-8 cyclohexyl(pyrrolidin-1-yl)methanone 
• 7103-46-0 N-(cyclohexanecarbonyl)piperidine 

Downstream Products

• 4664-71-5 Cyclohexyl-<3-Chlor-4-dimethylamino-phenyl>-keton 
• 4779-38-8 Cyclohexyl-<4-dimethylamino-phenyl>-keton-N-oxid 

Relevant academic research and scientific papers

Vinyl Triflate–Aldehyde Reductive Coupling–Redox Isomerization Mediated by Formate: Rhodium-Catalyzed Ketone Synthesis in the Absence of Stoichiometric Metals

Direct conversion of aldehydes to ketones is achieved via rhodium-catalyzed vinyl triflate-aldehyde reductive coupling-redox isomerization mediated by potassium formate. This method circumvents premetalated C-nucleophiles and discrete redox manipulations typically required to form ketones from aldehydes.

Nickel-Mediated Photoreductive Cross Coupling of Carboxylic Acid Derivatives for Ketone Synthesis**

A simple visible light photochemical, nickel-catalyzed synthesis of ketones from carboxylic acid-derived precursors is presented. Hantzsch ester (HE) functions as a cheap, green and strong photoreductant to facilitate radical generation and also engages in the Ni-catalytic cycle to restore the reactive species. With this dual role, HE allows for the coupling of a large variety of radicals (1°,2°, benzylic, α-oxy & α-amino) with aroyl and alkanoyl moieties, a new feature in reactions of this type. With both precursors deriving from abundant carboxylic acids, this protocol is a welcome addition to the organic chemistry toolbox. The reaction proceeds under mild conditions without the need for toxic metal reagents or bases and shows a wide scope, including pharmaceuticals and complex molecular architectures.

P -Selective (sp2)-C-H functionalization for an acylation/alkylation reaction using organic photoredox catalysis

p-Selective (sp2)-C-H functionalization of electron rich arenes has been achieved for acylation and alkylation reactions, respectively, with acyl/alkylselenides by organic photoredox catalysis involving an interesting mechanistic pathway.