128886-84-0

Upstream product

• 106-48-9 4-chloro-phenol 
• 98-74-8 4-Nitrobenzenesulfonyl chloride 
• 30362-87-9 p-Nitrophenyl p-nitrobenzenesulphonate 
• 24573-38-4 4-chlorophenolate 

Downstream Products

• 138-42-1 p-nitrobenzenesulfonic acid 
• 13159-74-5 4-chloro-N-(4-chlorobenzyl)aniline 
• 106-48-9 4-chloro-phenol 
• 73842-46-3 N-[(4-methylphenyl)methyl]-4-chloroaniline 
• 1417547-18-2 4-chlorophenyl 4-(3-(2,6-difluorobenzoyl)ureido)benzenesulfonate 
• 24573-38-4 4-chlorophenolate 
• 2948-37-0 N-(4-chlorophenyl)benzylamine 
• 52374-25-1 N-benzyl-4-nitrobenzenesulfonamide 
• 104329-18-2 N-(4-chlorophenyl)-4-methoxybenzenemethanamine 
• 171414-17-8 N-[(4-methoxyphenyl)methyl]-4-nitro-benzenesulfonamide 

Relevant academic research and scientific papers

Kinetic study on alkaline hydrolysis of Y-substituted phenyl X-substituted benzenesulfonates: Effects of changing nucleophile from azide to hydroxide ion on reactivity and transition-state structure

Second-order rate constants (kOH-) for alkaline hydrolysis of 2,4-dinitrophenyl X-substituted benzenesulfonates (1a-1f) and Y-substituted phenyl 4-nitrobezenesulfonates (2a-2g) have been measured spectrophotometrically. Comparison of kOH/

Design, synthesis, and insecticidal evaluation of new benzoylureas containing amide and sulfonate groups based on the sulfonylurea receptor protein binding site for diflubenzuron and glibenclamide

On the basis of the sulfonylurea receptor (SUR) protein binding site for diflubenzuron and glibenclamide, 15 new benzoylphenylureas containing amide and sulfonate groups were designed and synthesized. Their structures were characterized by 1H n

Competitive Reaction Pathways in the Nucleophilic Substitution Reactions of Aryl Benzenesulfonates with Benzylamines in Acetonitrile

The reactions of aryl benzenesulfonates (YC6H4SO2OC6H4Z) with benzylamines (XC6H4CH2NH2) in acetonitrile at 65.0 deg C have been studied. The reactons proceed competitevely by S-O (kS-O) and C-O (kC-O) bond scission, but the former provides the major reaction pathway. On the basis of analysis of the Hammet and Broensted coefficients together with the cross-interaction constants ρXY, ρYZ, and ρXZ, stepwise mechanisms are proposed in which the S-O bond cleavage proceeds by rate-limiting formation of a trigonal-bipyramidal pentacoordinate (TBP-5C) intermediate, whereas the C-O bond scission takes place by rate-limiting expulsion of the sulfonate anion (YC6H4SO3-) from a Meisenheimer-type complex.

Retardation of Hydrolysis of Aryl Arenesulphonate Esters by Quinuclidine through Complex Formation

The hydrolysis of aryl arenesulphonate esters is considerably retarded upon the addition of quinuclidine (Quin).Kinetic and spectral data indicate that the protonated form of Quin forms non-covalent complexes with the sulphonate esters and that the comple