135365-33-2

Upstream product

• 65972-30-7 3-(n-octadecyloxy)aniline 
• 79410-29-0 5-(chloroformyl)-cis,cis-1,3,5-trimethylcyclohexane-1,3-dicarboxylic anhydride 
• 135365-32-1 5-<<3-(octadecyloxy)phenyl>carbamoyl>-cis,cis-1,3,5-trimethylcyclohexane-1,3-dicarboxylic anhydride 
• 112-89-0 1-Bromooctadecane 
• 621-42-1 meta-hydroxyacetanilide 
• 135365-30-9 3-(octadecyloxy)acetanilide 
• 79410-20-1 Kemp's triacid 

Relevant academic research and scientific papers

Molecular recognition at the air-water interface. Specific binding of nitrogen aromatics and amino acids by monolayers of long-chain derivatives of Kemp's acid

Long-chain derivatives of Kemp's acid formed stable monolayers at the air-water interface, where the carboxylic acid groups produced the cyclic dimer species and served as a molecular cleft for specific binding of nitrogen aromatics and amino acids. The s

Molecular Recognition at the Interface. Synthesis and Monolayer Property of Long-Chain Derivatives of Kemp's Acid

Monolayer formation of octadecyl derivatives of a cyclohexanetricarboxylic acid (Kemp's acid) was examined.A symmetrically substituted double-chain derivative gave a stable monolayer in which carboxylic acids formed cyclic dimers at the air-water interfac