20834-66-6

Upstream product

• 20168-72-3 4-nitrophenyl phenyl disulfide 
• 97-00-7 1-chloro-2,4-dinitro-benzene 
• 64-17-5 ethanol 
• 854877-49-9 biphenyl-4-yl-(4-nitro-phenyl)-disulfide 
• 1849-36-1 para-nitrobenzenethiol 
• 100-25-4 para-dinitrobenzene 
• 13113-79-6 sodium 4-nitrobenzenethiolate 

Downstream Products

• 1098-16-4 (2,4-dinitro-phenyl)-(4-nitro-phenyl)-sulfone 
• 108014-09-1 (4-acetylamino-phenyl)-(2,4-bis-acetylamino-phenyl)-sulfide 
• 14314-69-3 potassium 2,4-dinitrophenolate 
• 71367-29-8 4-nitro-thiophenol potassium salt 
• 1043-55-6 2,4-dinitrophenyl p-nitrophenyl sulfoxide 

Relevant academic research and scientific papers

A highly selective fluorescent probe for thiophenols

A rapid response to thiophenols is obtained with probe 1 (see scheme), which induces a significant (> 50-fold) fluorescence enhancement as a result of cleavage of the electron-withdrawing moiety, thus generating strongly fluorescent molecule 2. No fluores

Contribution of linear free energy relationships to isozyme- and pH-dependent substrate selectivity of glutathione S-transferases: Comparison of model studies and enzymatic reactions

A novel application of linear free energy relationships is described in which the substrate selectivities and pH dependencies of glutathione S-transferases (GSTs) are correlated to the pK(a), of glutathione (GSH) at the active site. To determine whether t