103440-03-5

Basic information

• Product Name: 3-nitro-(4-chloromethyl) benzoic acid
• Synonyms: 3-nitro-(4-chloromethyl) benzoic acid
• CAS NO: 103440-03-5
• Molecular Weight: 215.593
• Mol File: 103440-03-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-nitro-(4-chloromethyl) benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-nitro-(4-chloromethyl) benzoic acid(103440-03-5)
• EPA Substance Registry System: 3-nitro-(4-chloromethyl) benzoic acid(103440-03-5)

Safety Data

• Hazardous Substances Data: 103440-03-5(Hazardous Substances Data)

Upstream product

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

Downstream Products

• 103440-02-4 4-<(2'-Carboxyphenylsulfonyl)methyl>-3-nitrobenzoic acid 
• 103439-98-1 4-<(4'-Aminophenylsulfonyl)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 
• 150713-35-2 Ethyl 2-<2-amino-4-(ethoxycarbonyl)phenyl>benzothiophene-6-carboxylate 

Relevant articles and documents

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

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.