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Usage

Uses

Used in Pharmaceutical Industry:
2-(4-methoxybenzoyl)cyclohexanone is used as a building block for the synthesis of various pharmaceuticals due to its anti-inflammatory, antitumor, and antimicrobial properties, contributing to the development of new therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(4-methoxybenzoyl)cyclohexanone serves as a key intermediate in the production of agrochemicals, leveraging its biological activities to enhance crop protection and management.
Used in Fragrance and Flavoring Industry:
2-(4-methoxybenzoyl)cyclohexanone is utilized as a versatile intermediate in the creation of fragrances and flavoring agents, capitalizing on its ability to contribute to the unique scents and tastes in various consumer products.
Used in Organic Synthesis:
As a reagent in organic synthesis, 2-(4-methoxybenzoyl)cyclohexanone is employed for the preparation of natural products and other organic compounds, highlighting its synthetic utility across different chemical domains.

Upstream product

• 108-94-1 cyclohexanone 
• 100-07-2 4-methoxy-benzoyl chloride 
• 34434-35-0 Natrium-Verbindung des Cyclohexanons 
• 670-80-4 4-cyclohexen-1-ylmorpholine 
• 930-68-7 cyclohexenone 
• 105-13-5 4-Methoxybenzyl alcohol 

Downstream Products

• 26860-96-8 cis-α-(p-Methoxyphenyl)-2-(cyclohexylamino)-cyclohexanmethanol 
• 13724-58-8 cis-A-α-(p-Methoxyphenyl)-2-(methylamino)-cyclohexanmethanol 
• 81581-50-2 3-Methoxy-1-(4-methoxy-phenyl)-isoquinoline-4-carbonitrile 
• 81581-45-5 3-Methoxy-1-(4-methoxy-phenyl)-5,6-dihydro-isoquinoline-4-carbonitrile 
• 81581-41-1 3-Methoxy-1-(4-methoxy-phenyl)-5,6,7,8-tetrahydro-isoquinoline-4-carbonitrile 
• 81581-48-8 3-Methoxy-1-(4-methoxy-phenyl)-1,2-dihydro-isoquinoline-4-carbonitrile 
• 81581-43-3 3-Methoxy-1-(4-methoxy-phenyl)-8-oxo-5,6,7,8-tetrahydro-isoquinoline-4-carbonitrile 
• 345307-80-4 8-Hydroxy-3-methoxy-1-(4-methoxy-phenyl)-5,6,7,8-tetrahydro-isoquinoline-4-carbonitrile 
• 28344-02-7 N-{(1R,2S)-2-[Hydroxy-(4-methoxy-phenyl)-methyl]-cyclohexyl}-N-(4-methoxy-phenyl)-acetamide 
• 144296-25-3 5-(4-methoxyphenyl)-6,7,8,9-tetrahydro-3H-pyrazolo[3,4-c]isoquinolin-1-amine 
• 144296-31-1 3-chloro-1-(4-methoxyphenyl)-5,6,7,8-tetrahydroisoquinoline-4-carbonitrile 
• 28343-80-8 cis-A-α-(p-Methoxyphenyl)-2-(methylamino)-cyclohexanmethanol-benzoatester 
• 28343-79-5 cis-A-α-(p-Methoxyphenyl)-2-(N-methylbenzamido)-cyclohexanmethanol 
• 42427-54-3 2-bromo-6-(4-methoxy-benzoyl)-cyclohexanone 

Relevant academic research and scientific papers

Iridium-catalyzed reaction of enones with alcohols affording 1,3-diketones

An iridium-catalyzed coupling reaction of alcohols with enones has been successfully developed providing access to 1,3-diketones with high selectivity in good yields. This reaction provides an atom-economical route to 1,3-diketones from readily available

Regiochemistry of the condensation of 2-aroyl-cyclohexanones and 2-cyanoacetamide: 13C-labeling studies and semiempirical MO calculations

Hydroxy-aryl-5,6,7,8-tetrahydroisoquinoline-4-carbonitriles represent interesting chemical scaffolds, but synthetic access to these compounds is limited. The reaction of 2-aroyl-cyclohexanones with 2-cyanoacetamide and base in ethanol has been reported to

Fragment based lead discovery of small molecule inhibitors for the EPHA4 receptor tyrosine kinase

The in silico identification, optimization and crystallographic characterization of a 6,7,8,9-tetrahydro-3H-pyrazolo[3,4-c]isoquinolin-1-amine scaffold as an inhibitor for the EPHA4 receptor tyrosine kinase is described. A database containing commercially

1,3-Diketones from acid chlorides and ketones: A rapid and general one-pot synthesis of pyrazoles

1,3-Diketones were synthesized directly from ketones and acid chlorides and were then converted in situ into pyrazoles by the addition of hydrazine. This method is extremely fast, general, and chemoselective, allowing for the synthesis of previously inaccessible pyrazoles and synthetically demanding pyrazole-containing fused rings.

Synthesis of Isomeric Series of Aryltetrahydrobenzisoxazoles and Arylcyclopentisoxazoles

Four series of potential PAF-antagonists in which the isoxazole nucleus is condensed with a polyhydrogenated five- or six-carbon ring were prepared.The synthesis of the compounds 3-aryl-4,5,6,7-tetrahydrobenzisoxazoles 1, 3-arylcyclopentisoxazole 2,