3277-80-3

Basic information

• Product Name: 4-CHLOROPHENYL CYCLOHEXYL KETONE
• Synonyms: 4-CHLOROPHENYL CYCLOHEXYL KETONE;Cyclohexyl(4-chlorophenyl)methanone;OTAVA-BB 1044135;UKRORGSYN-BB BBV-5118695;(4-chlorophenyl)(cyclohexyl)Methanone
• CAS NO: 3277-80-3
• Molecular Formula: C₁₃H₁₅ClO
• Molecular Weight: 222.71
• Mol File: 3277-80-3.mol
• Article Data: 23

Chemical Properties

• Melting Point: 61.5-62.5 °C
• Boiling Point: 337.38°C at 760 mmHg
• Flash Point: 186.552°C
• Appearance: /
• Density: 1.14g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.55
• CAS DataBase Reference: 4-CHLOROPHENYL CYCLOHEXYL KETONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-CHLOROPHENYL CYCLOHEXYL KETONE(3277-80-3)
• EPA Substance Registry System: 4-CHLOROPHENYL CYCLOHEXYL KETONE(3277-80-3)

Safety Data

• Hazardous Substances Data: 3277-80-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H15ClO/c14-12-8-6-11(7-9-12)13(15)10-4-2-1-3-5-10/h6-10H,1-5H2

Upstream product

• 41253-21-8 sodium triazole 
• 129500-95-4 (1R,2R)-2-Bromo-1-(4-chloro-phenyl)-cycloheptanol 
• 104-88-1 4-chlorobenzaldehyde 
• 110-83-8 cyclohexene 
• 100-52-7 benzaldehyde 
• 110-82-7 cyclohexane 
• 201230-82-2 carbon monoxide 
• 10557-71-8 4-chlorophenyltrimethylsilane 
• 80783-98-8 N-methoxy-N-methylcyclohexanecarboxamide 
• 873-77-8 (4-chlorphenyl)magnesium bromide 
• 2719-27-9 cyclohexanylcarbonyl chloride 
• 77826-33-6 1-p-Chlorphenylcycloheptanol 
• 120568-01-6 1-(4-chlorophenyl)cyclohept-1-ene 
• 502-42-1 cycloheptanone 

Downstream Products

• 93765-49-2 (4-Chloro-phenyl)-cyclohexyl-pyrimidin-5-yl-methanol 
• 128352-35-2 methyl E-2-(o-carboxyphenyl)-3-cyclohexyl-p-chlorocinnamate 
• 128352-41-0 methyl Z-2-(o-carboxyphenyl)-3-cyclohexyl-p-chlorocinnamate 
• 1029548-00-2 4-chloromethyl-2-(4-chloro-phenyl)-2-cyclohexyl-[1,3]dioxolane 
• 868396-33-2 3-(4-chloro-phenyl)-3-cyclohexyl-3-hydroxy-1-piperidin-1-yl-propan-1-one 
• 128352-47-6 4-[1-(4-Chloro-phenyl)-1-cyclohexyl-meth-(Z)-ylidene]-isochroman-1,3-dione 
• 128352-54-5 6-chloro-2-(o-carboxyphenyl)-3-cyclohexylind-2-enone lactone 
• 128352-38-5 2-[(E)-1-Carboxy-2-(4-chloro-phenyl)-2-cyclohexyl-vinyl]-benzoic acid 
• 128352-44-3 2-[(Z)-1-Carboxy-2-(4-chloro-phenyl)-2-cyclohexyl-vinyl]-benzoic acid 
• 1233012-05-9 (Pd(C₆H₃ClCO(cyclo-C₆H₁₁)))2(trifluoroacetate)2 

Relevant articles and documents

Cobalt-Catalyzed Markovnikov-Selective Radical Hydroacylation of Unactivated Alkenes with Acylphosphonates

Acylphosphonates having the 5,5-dimethyl-1,3,2-dioxophosphinanyl skeleton are developed as efficient intermolecular radical acylation reagents, which enable the cobalt-catalyzed Markovnikov hydroacylation of unactivated alkenes at room temperature under mild conditions. The protocol exhibits broad substrate scope and wide functional group compatibility, providing branched ketones in satisfactory yields. A mechanism involving the Co-H mediated hydrogen atom transfer and subsequent trapping of alkyl radicals by acylphosphonates is proposed.

Site-Selective C–H Benzylation of Alkanes with N-Triftosylhydrazones Leading to Alkyl Aromatics

-

Method for synthesizing aryl ketone compound by taking AQ as photocatalyst

The invention provides a method for synthesizing an aryl ketone compound by taking AQ as a photocatalyst. The method comprises the following steps that AQ serves as a photocatalyst; under the conditions of a palladium catalyst, a phosphine ligand, weak base and an organic solvent, a 390-to-430-nm photocatalysis lamp is used for irradiation at room temperature in an inert protective atmosphere, soan aldehyde group-containing compound reacts with Ar-X, wherein Ar-X is aryl halide or aryl trifluoromethanesulfonic acid, the aryl halide is aryl bromide or aryl iodide, and the aldehyde group-containing compound is one selected from aryl aldehyde, alkyl aldehyde, linear primary aldehyde and acyclic secondary aldehyde. According to the invention, the anthraquinone (AQ) HAT photocatalyst and palladium catalyst are combined for use, C-H arylation and alkenylation reactions of aldehyde can be directly carried out to synthesize ketone, and reaction efficiency is high. The method has the advantages of mild reaction conditions, high yield and a wide substrate application range, and can be used for synthesizing natural products in medicinal plants.