83487-65-4

Upstream product

• 83487-64-3 C₄₈H₄₂O₈ 
• 106-96-7 propargyl bromide 
• 826-55-1 2-methyl-2-phenylpropionic acid 
• 92-70-6 3-Hydroxy-2-naphthoic acid 
• 26513-28-0 sodium 2-carboxy-3-hydroxy-7-naphthalenesulfonate 
• 83487-62-1 neophyl 3-(MEMoxy)-7-(propargyloxy)-2-naphthoate 
• 83487-63-2 neophyl 3-hydroxy-7-(propargyloxy)-2-naphthoate 
• 83487-61-0 3-(2-Methoxy-ethoxymethoxy)-7-prop-2-ynyloxy-naphthalene-2-carboxylic acid 
• 83487-46-1 n-hexyl 3-hydroxy-7-(propargyloxy)-2-naphthoate 
• 83487-45-0 n-hexyl 3,7-dihydroxy-2-naphthoate 
• 83511-07-3 3,7-dihydroxy-2-naphthoic acid 
• 2901-13-5 ethyl 2-methyl-2-phenylpropionate 
• 2173-69-5 2-methyl-2-phenyl-propan-1-ol 

Downstream Products

• 83487-67-6 C₅₄H₆₀O₈ 
• 83487-66-5 1,8,17,24-tetraoxa<8.8>(2,6)-naphthalenophane-3,5,19,21-tetrayne-10,30-dicarboxylic acid dineophyl ester 

Relevant academic research and scientific papers

1,8,17,24-Tetraoxa(2,6)naphthalenophane-3,5,19,21-tetrayne-10,13-dicarboxylic Acid Derivatives, Novel Complexors of Aromatic Guests

Synthesis and complexation behavior of the title molecules are described.Study of aromatic solvent induced shifts of these molecules support the contention that their large cavity can accomodate aromatic rings.The behavior of acid 1a in water suggests that this effect enhanced in aqueous medium, as is expected for formation of hydrophobic inclusion complexes.In contrast to the rigid naphthalenophanes (1), their saturated derivatives (7) exist in a collapsed conformation and do not incorporate aromatic guests.