35889-00-0

Usage

InChI:InChI=1/C14H18O2/c15-14(16)10-11-6-8-13(9-7-11)12-4-2-1-3-5-12/h6-9,12H,1-5,10H2,(H,15,16)

Upstream product

• 29030-58-8 (4-cyclohexyl-phenyl)-acetonitrile 
• 72825-30-0 4'-cyclohexyl-2-chloroacetophenone 
• 7601-90-3 perchloric acid 
• 65152-27-4 4-cyclohexyl-mandelic acid 
• 64-19-7 acetic acid 
• 4463-31-4 4-cyclohexylbenzyl chloride 
• 827-52-1 1-phenyl-1-cyclohexane 
• 15719-64-9 methylammonium carbonate 
• 39154-65-9 (4-cyclohexyl-phenyl)-glyoxylic acid ethyl ester 

Downstream Products

• 61578-80-1 (4-cyclohexyl-phenyl)-acetyl chloride 
• 59182-69-3 [2-(4-Cyclohexyl-phenyl)-1-methyl-ethyl]-(3,3-diphenyl-propyl)-amine 
• 29677-27-8 (4-cyclohexyl-phenyl)-acetic acid amide 
• 130497-48-2 2-(4-Cyclohexyl-phenyl)-1-(2-pyrrolidin-1-ylmethyl-piperidin-1-yl)-ethanone 
• 59182-66-0 4-Cyclohexylphenylaceton 

Relevant academic research and scientific papers

Media controlled photo - Favorskii type rearrangement of α-chloro acetophenones: Synthesis of phenylacetic acids

Photolysis of substituted α-chloro acetophenones has been studied in different solvent systems wherein 1,2-aryl migration is found to be media controlled. Effect of substituents on the migratory aptitude and a direct access to phenylacetic acids, in practical yields, has been described.