103440-03-5

Upstream product

• 874-86-2 4-cyanobenzyl chloride 
• 99-94-5 p-Toluic acid 
• 1642-81-5 p-(chloromethyl)benzoic acid 
• 7499-07-2 4-chloro-2-methylbenzoic acid 

Downstream Products

• 150713-16-9 Ethyl 4-(chloromethyl)-3-nitrobenzoate 
• 103439-98-1 4-<(4'-Aminophenylsulfonyl)methyl>-3-nitrobenzoic acid 
• 103440-02-4 4-<(2'-Carboxyphenylsulfonyl)methyl>-3-nitrobenzoic acid 
• 150713-29-4 C₂₆H₂₈O₆S₄ 
• 150713-31-8 Diethyl 2-<(ethoxythiocarbonyl)thio>-2'-nitrostilbene-4,4'-dicarboxylate 
• 150713-19-2 Diethyl 2,2'-diazido-(E)-stilbene-4,4'-dicarboxylate 
• 150713-30-7 C₂₂H₁₈N₂O₄Se₂ 
• 150713-33-0 Diethyl 2-nitro-2'-(selenocyanato)-(E)-stilbene-4,4'-dicarboxylate 
• 150713-15-8 diethyl 2,2'-dinitro-(E)-stilbene-4,4'-dicarboxylate 
• 150713-34-1 Ethyl 2-<4-(ethoxycarbonyl)-2-nitrophenyl>benzoselenophene-6-carboxylate 
• 150713-32-9 Ethyl 2-<4-(ethoxycarbonyl)-2-nitrophenyl>benzothiophene-6-carboxylate 
• 150713-36-3 2-(4-Ethoxycarbonyl-2-selenocyanato-phenyl)-benzo[b]thiophene-6-carboxylic acid ethyl ester 
• 150713-18-1 Diethyl 2-amino-2'-nitro-(E)-stilbene-4,4'-dicarboxylate 
• 150713-17-0 diethyl 2,2'-diamino-(E)-stilbene-4,4'-dicarboxylate 

Relevant academic research and scientific papers

Study of a new 3D MOF and its adsorption, slow release and biological activity in water-soluble and oil-soluble pesticides

The ligands of (E)-bis(p-3-nitrobenzoic acid) vinyl (C16H10N2O8) were synthesized in three steps, and then the MOF-Zn2(EBNB)2(BPY)2·2H2O was synthesized by solvotherma

Enhancement of Gas Sorption and Separation Performance via Ligand Functionalization within Highly Stable Zirconium-Based Metal-Organic Frameworks

By using a modulated synthetic strategy, three isostructural Zr-based metal organic frameworks [Zr6O4(OH)4(EDDC)6] (JLU-Liu34), [Zr6O4(OH)4(EDDC-NO2)6] (JLU

Kinetics of the reaction of sodium arylthiolates with nitro-carboxybenzyl halide derivatives

The rate constants for the reactions of 4-halomethyl-3-nitrobenzoic acids, the nonnitro derivatives, and their ethyl esters with arylthiolates were measured at different temperatures. It was found that the retardation in rate constants compared to benzyl halides is due to the electrostatic repulsion between the electronegative substituents (COO- and/or NO2) in the substrates and thiolate ions Good correlations between log K2 values of the acids and carbon basicities of thiolates were found while log k2 values of the esters show good straight lines with Hammett a constants, pKa. and carbon basicities of arylthiolates.

Synthesis and Properties of Diethyl 5,10-Dihetera-5,10-dihydroindenoindene-2,7-dicarboxylates

A series of six heterocyclic diesters 1b-6b containing all combinations of nitrogen, sulfur, and selenium has been prepared from a common precursor, diethyl 2,2'-dinitrostilbene-4,4'-dicarboxylate.Electrochemical analysis showed oxidation potential increases in the order NA liquid crystals.A new synthetic method leading to the indoloindazole ring system has been found.