1915-01-1

Upstream product

• 843-55-0 1,1-bis(p-hydroxyphenyl)cyclohexane 
• 79-11-8 chloroacetic acid 
• 108-94-1 cyclohexanone 
• 3926-62-3 sodium monochloroacetic acid 
• 181467-87-8 {4-[1-(4-Ethoxycarbonylmethoxy-phenyl)-cyclohexyl]-phenoxy}-acetic acid ethyl ester 

Downstream Products

• 181467-87-8 {4-[1-(4-Ethoxycarbonylmethoxy-phenyl)-cyclohexyl]-phenoxy}-acetic acid ethyl ester 

Relevant academic research and scientific papers

Extractant as well as preparation method and application thereof

The invention relates to the technical field of rare earth recovery, and discloses an extraction agent and a preparation method and application of the extraction agent. The extraction agent is a novelextraction agent with a dicarboxylic acid structure, an

Synthesis and spectral study of R,R′,4,4′-cyclohexylidene diphenyloxy acetic acids with antimicrobial activity

Synthesis of R,R′,4,4′-cyclohexylidene diphenyloxy acetic acids (R,R′=H,CH3and Cl) by dissolving 0.1 mole bisphenols in 0.4 mole sodim hydroxide with drop wise addition of 0.2 mole chloroacetic acid. The reaction mixture refluxed for 4h at 60°C. Phenoxy acids have been confirmed by IR and NMR spectral characterization. The acids are also characterized by their antimicrobial and antifungal activities. The activities have been interpreted in light of bisphenol structures and the nature of substituent(s). The wide scale uses of bisphenol bioactive agents have brought many advantages to the agricultural industries.

Thermal and alkali-catalyzed hydrolysis study of R,R′,4,4′ -cyclohexylidenediphenyloxyacetic acids and their ethyl esters

R,R′,4,4′-Cyclohexylidenediphenyloxyacetic acid (PAAC-1 to PAAC-7, R = H, CH3, Cl, Br, NO2 and R′ = H, Cl, Br, NO2) are thermally stable up to 226-320°. Kinetic parameters are interpreted in light of the nature of the subs