42823-73-4

Upstream product

• 1129-35-7 4-cyanobenzoic acid methyl ester 

Downstream Products

• 123704-58-5 4-(5-Methyl-pyrimidin-2-yl)-benzoic acid methyl ester 
• 340736-87-0 methyl 4-(5-oxo-4,5-dihydro-1,2,4-thiadiazol-3-yl)benzoate 
• 135321-84-5 methyl 4-(N-{[(2-methyl-2-propanyl)oxy]carbonyl}carbamimidoyl)benzoate 
• 104631-92-7 4-(5-(4'butylphenyl)pyrimidine-2-yl) benzoic acid 2'-dodecyloxypropyl ester 
• 1450790-57-4 methyl 4-(4-Oxo-4,5,7,8-tetrahydro-3H-pyrano[4,3-d]pyrimidin-2-yl)benzoate 
• 123704-55-2 C₃₆H₄₀N₂O₄ 
• 123704-56-3 C₃₂H₂₉N₃O₄ 
• 123704-57-4 2-Chloro-4-[4-(5-heptyl-pyrimidin-2-yl)-benzoyloxy]-benzoic acid 4-cyano-phenyl ester 
• 123704-53-0 C₃₄H₃₆N₂O₄ 
• 123704-54-1 5-Cyanophenyl p-benzoate 
• 108768-42-9 4-(5-Heptyl-pyrimidin-2-yl)-benzoic acid 3-chloro-4-cyano-phenyl ester 
• 123704-50-7 4-(5-Heptyl-pyrimidin-2-yl)-benzoic acid 4-pentyl-phenyl ester 
• 123704-52-9 4-(5-Heptyl-pyrimidin-2-yl)-benzoic acid 4-cyano-phenyl ester 
• 123704-63-2 4-(5-Pentyl-pyrimidin-2-yl)-benzoic acid 4-chlorocarbonyl-phenyl ester 

Relevant academic research and scientific papers

A Substituent Chemical Shift (SCS) Effect Study by 13C and 19F NMR of para-Substituted Phenylhalodiazirines

A range of 3-(para-substituted-phenyl)-3-halodiazirines have been prepared and their 13C and 19F NMR spectra measured.Calculated with these data were the susceptibility coefficients ρ1 and ρR of the inductive (?1) and resonance (?R0) effects, respectively, to substituent-induced chemical shift differences at the diazirine carbon (13C NMR) and the 3-fluorine(19F NMR of the 3-fluorodiazirine series).An inverse relationship was found between the suceptibility parameters and the electronegativity of the halo substituent at the diazirine carbon. KET WORDS - 13C NMR 19F NMR substituent induced chemical shifts p-substituted phenylhalodiazirines