14451-58-2

Usage

Uses

Used in Pharmaceutical Industry:
Ethanone, 1-(3-chloro-4-cyclohexylphenyl)is used as a building block for the synthesis of other organic compounds, particularly in the pharmaceutical industry. Its unique structural features, including the cyclohexyl and chlorine groups, may impart specific properties and reactivity that are beneficial for the development of new drugs and therapeutic agents.
Used in Chemical Reactions:
Ethanone, 1-(3-chloro-4-cyclohexylphenyl)is used as a reactant in various chemical reactions due to its ketone derivative nature and the presence of the cyclohexyl and chlorine groups. These groups may allow for specific reactivity patterns that can be exploited in the synthesis of other compounds or in the modification of existing molecules.
Used in Biological Studies:
Ethanone, 1-(3-chloro-4-cyclohexylphenyl)may be used in biological studies to investigate its interactions with biological systems, such as enzymes or receptors. The unique structural features of the compound may provide insights into its potential biological activity and possible applications in the development of new therapeutic agents or diagnostic tools.

Upstream product

• 18594-05-3 4-cyclohexylacetophenone 
• 827-52-1 1-phenyl-1-cyclohexane 
• 13376-20-0 1-(4-cyclohexyl-3-nitrophenyl)ethanone 
• 110-82-7 cyclohexane 
• 99-02-5 3'-Chloroacetophenone 
• 17641-82-6 1-(3-amino-4-cyclohexylphenyl)ethanone 

Downstream Products

• 59721-35-6 2-(p-Cyclohexyl-m-chlorphenyl)-2-penten-4-on 
• 38258-61-6 4-(3-Chlor-4-cyclohexylphenyl)-4-oxo-crotonsaeure 
• 67601-29-0 3-Chloro-4-cyclohexyl-phenol 
• 59721-35-6 (e)-4-(3-chloro-4-cyclohexyl-phenyl)-3-pentene-2-one 
• 52506-86-2 3-chloro-4-cyclohexyl-1-ethynylbenzene 
• 37049-95-9 hydrochloride of 3-chloro 4-cyclohexyl α-methyl benzylamine 
• 56759-89-8 3-chloro-4-cyclohexyl-1-(3-diethylamino-1-oxo-propyl)-benzene 
• 103-69-5 N-ethyl-N-phenylamine 
• 42601-80-9 3-chloro-4-cyclohexylbenzoic acid 
• 1403233-98-6 {4-[5-(3-chloro-4-cyclohexylphenyl)-[1,2,4]-oxadiazol-3-yl]phenyl}methanol 
• 1403233-99-7 5-(3-chloro-4-cyclohexylphenyl)-3-(4-chloromethylphenyl)-[1,2,4]-oxadiazole 
• 1403234-00-3 4-methyl-1-{4-[5-(3-chloro-4-cyclohexylphenyl)-[1,2,4]-oxadiazol-3-yl]benzyl}piperidine-4-carboxylic acid ethyl ester 
• 1403232-15-4 1-{4-[5-(3-chloro-4-cyclohexylphenyl)-[1,2,4]-oxadiazol-3-yl]benzyl}-4-methylpiperidine-4-carboxylic acid 

Relevant academic research and scientific papers

Nickel-Catalyzed, para-Selective, Radical-Based Alkylation of Aromatic Ketones

A direct, para-selective, radical-based alkylation of aromatic ketones with alkanes has been developed using a nickel catalyst with oxamide as the ligand. Acetophenones bearing electron-withdrawing substituents were functionalized directly with simple alkanes with high para-selectivity while acetophenones with electron-donating groups were mainly para-functionalized. A mechanistic study indicated that C-H bond activation of the aromatic ring may be the rate-determining step of the reaction.

Preparation method of 4-cycloalkylacetophenone derivatives

The invention discloses a preparation method of 4-cycloalkylacetophenone derivatives, and belongs to the technical field of organic compounds. A 2-substituted acetophenone derivative or a 3-substituted acetophenone derivative is used as an initiator, so raw materials are easy to obtain and have many kinds; and the 4-substituted cycloalkyl acetophenone derivatives obtained by using the method are various, can be directly used, and can also be used in other further reactions. The preparation method has the advantages of simplicity in reaction operation and post-treatment, high yield, and no generation of a large amount of metal salts, is a green method with high atom economy, and is suitable for large-scale production.

Novel piperidinyl monocarboxylic acids as S1P1 receptor agonists

The present invention relates to novel compounds acting as agonists at S1P (sphingosine-1-phosphate) receptors, compositions containing these compounds, use of these compounds in medicine and their process of preparation.

NOVEL PIPERIDINYL MONOCARBOXYLIC ACIDS AS S1P1 RECEPTOR AGONISTS

The present invention relates to novel compounds acting as agonists at S1P (sphingosine-1-phosphate) receptors, compositions containing these compounds, use of these compounds in medicine and their process of preparation.