1523-21-3

Basic information

• Product Name: 4-nitrophenyl 3,5-dinitrobenzoate
• Synonyms: 4-nitrophenyl 3,5-dinitrobenzoate
• CAS NO: 1523-21-3
• Molecular Weight: 333.214
• Mol File: 1523-21-3.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 4-nitrophenyl 3,5-dinitrobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-nitrophenyl 3,5-dinitrobenzoate(1523-21-3)
• EPA Substance Registry System: 4-nitrophenyl 3,5-dinitrobenzoate(1523-21-3)

Safety Data

• Hazardous Substances Data: 1523-21-3(Hazardous Substances Data)

Upstream product

• 100-02-7 4-nitro-phenol 
• 99-34-3 3,5-dinitrobenzoic acid 
• 99-33-2 3,5-dinitrobenoyl chloride 

Downstream Products

• 100-02-7 4-nitro-phenol 
• 2900-63-2 3,5-dinitrobenzohydrazide 
• 57499-86-2 1-(3,5-dinitro-benzoyl)-piperidine 
• 133339-10-3 (3,5-dinitrophenyl)morpholinylmethanone 
• 42824-44-2 piperidinium 4-nitrophenolate 
• 38144-19-3 4-chlorophenyl 3,5-dinitrobenzoate 
• 1037569-82-6 N-[N-(3,5-dinitro-benzoyl)-glycyl]-glycine 
• 1523-20-2 phenyl 3,5-dinitrobenzoate 
• 14609-74-6 p-nitrophenolate 
• 15573-49-6 3,5-dinitrobenzoate^(1-) 
• 99-34-3 3,5-dinitrobenzoic acid 
• 2782-41-4 N-butyl-3,5-dinitrobenzamide 

Relevant articles and documents

Alkaline Hydrolysis of 4-Nitrophenyl X-Substituted-Benzoates Revisited: New Insights from Yukawa–Tsuno Equation

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MOLECULAR TETRAHEDRON NANOCAGE, ITS PREPARATION, AND USES THEREOF

The present application is directed to a nanocage of Formula (I): wherein A and R are as described herein. The present application is also directed to a process for preparation of a nanocage of Formula (I). Methods of utilizing the nanocage for detecting an analyte in a fluid and for functionalizing a polymer are also described.

Evidence for a catalytic six-membered cyclic transition state in aminolysis of 4-nitrophenyl 3,5-dinitrobenzoate in acetonitrile: Comparative Br?nsted-type plot, entropy of activation, and deuterium kinetic isotope effects

A kinetic study for reactions of 4-nitrophenyl 3,5-dinitrobenzoate (1a) with a series of cyclic secondary amines in acetonitrile is reported. Plots of the pseudo-firstorder rate constant (kobsd) vs [amine] curve upward, while those of kobs