107151-39-3

Usage

InChI:InChI=1/C13H16O4/c1-17-12-8-4-2-6-10(12)11(14)7-3-5-9-13(15)16/h2,4,6,8H,3,5,7,9H2,1H3,(H,15,16)

Upstream product

• 100118-19-2 6-(2-hydroxybenzoyl)pentanoic acid 
• 77-78-1 dimethyl sulfate 
• 74-88-4 methyl iodide 
• 5720-06-9 2-Methoxyphenylboronic acid 
• 822-87-7 2-Chlorocyclohexanone 
• 2702-90-1 2-(2-methoxyphenyl)cyclohexan-1-one 

Downstream Products

• 854879-76-8 6-(5-amino-2-methoxy-phenyl)-6-oxo-hexanoic acid 
• 854879-20-2 6-(5-chloro-2-methoxy-phenyl)-6-oxo-hexanoic acid 
• 854876-80-5 6-(2-methoxy-5-nitro-phenyl)-6-oxo-hexanoic acid 

Relevant academic research and scientific papers

Selective C-C Bond Cleavage of Cycloalkanones by NaNO2/HCl

A novel selective fragmentation of cycloalkanones by NaNO2/HCl has been established. The C-C bond cleavage reaction proceeds smoothly under mild conditions, selectively affording versatile keto acids or oxime acids. The methodology can streamline the synthesis of valuable chiral molecules and isocoumarins from readily available feedstocks.

Visible Light-Driven, Copper-Catalyzed Aerobic Oxidative Cleavage of Cycloalkanones

A visible light-driven, copper-catalyzed aerobic oxidative cleavage of cycloalkanones has been presented. A variety of cycloalkanones with varying ring sizes and various α-substituents reacted well to give the distal keto acids or dicarboxylic acids with moderate to good yields.