92289-14-0

Basic information

• Product Name: 3-(4-nitrophenyl)pentanedioic acid
• Synonyms: Pentanedioic acid, 3-(4-nitrophenyl)-;3-(4-nitrophenyl)pentanedioic acid
• CAS NO: 92289-14-0
• Molecular Formula: C₁₁H₁₁NO₆
• Molecular Weight: 253.21
• Mol File: 92289-14-0.mol
• Article Data: 5

Chemical Properties

• Melting Point: 235 °C
• Boiling Point: 453.3°C at 760 mmHg
• Flash Point: 194.9°C
• Appearance: /
• Density: 1.458g/cm³
• Vapor Pressure: 5.24E-09mmHg at 25°C
• Refractive Index: 1.599
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 3.88±0.10(Predicted)
• CAS DataBase Reference: 3-(4-nitrophenyl)pentanedioic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-nitrophenyl)pentanedioic acid(92289-14-0)
• EPA Substance Registry System: 3-(4-nitrophenyl)pentanedioic acid(92289-14-0)

Safety Data

• Hazardous Substances Data: 92289-14-0(Hazardous Substances Data)

Usage

General Description

3-(4-nitrophenyl)pentanedioic acid is an organic compound with the chemical formula C11H9NO6. It is a dicarboxylic acid containing a nitrophenyl group attached to the third carbon of a pentanedioic acid molecule. 3-(4-nitrophenyl)pentanedioic acid is commonly used in organic synthesis and pharmaceutical research due to its potential applications in drug development. It is also known for its ability to form complexes with metal ions, making it useful in coordination chemistry. Additionally, 3-(4-nitrophenyl)pentanedioic acid is used as a reagent in analytical chemistry, particularly in the determination of metal ions in solution.

InChI:InChI=1/C11H11NO6/c13-10(14)5-8(6-11(15)16)7-1-3-9(4-2-7)12(17)18/h1-4,8H,5-6H2,(H,13,14)(H,15,16)

Upstream product

• 555-16-8 4-nitrobenzaldehdye 
• 340265-92-1 diethyl 2,4-diacetyl-3-(4-nitrophenyl)pentanedioate 
• 159088-58-1 C₉H₇NO₆ 
• 108-24-7 acetic anhydride 
• 1123-49-5 3,5-dimethyl-4-nitroisoxazole 
• 4165-96-2 3-phenylglutaric acid 
• 93711-15-0 5-hydroxy-5-methyl-3-(4-nitrophenyl)cyclohexanone-2,4-dicarboxylic acid diethyl ester 
• 7647-01-0 hydrogenchloride 
• 126989-14-8 tetraethyl 2-(4-nitrophenyl)propane-1,1,3,3-tetracarboxylate 
• 64-17-5 ethanol 
• 53911-69-6 3-(4-nitro-phenyl)-pentanedioic acid anhydride 

Downstream Products

• 954124-21-1 4-(4-nitrophenyl)piperidine-2,6-dione 
• 954124-90-4 1-methyl-4-(4-nitro-phenyl)-piperidine-2,6-dione 
• 1616787-08-6 3-(4-Nitro-phenyl)-pentanedioyl dichloride 
• 1616787-10-0 3-(4-aminophenyl)-1,5-bis(2,5-dimethylthiophen-3-yl)pentane-1,5-dione 
• 1616787-11-1 3-(4-(2,5-di(thiophen-2-yl)-1H-pyrrol-1-yl)phenyl)-1,5-bis(2,5-dimethylthiophen-3-yl)pentane-1,5-dione 
• 1616787-07-5 1-(4-[3,4-bis(2,5-dimethyl-3-thienyl)cyclopent-3-en-1-yl]phenyl)-2,5-di(2-thienyl)-1H-pyrrole 
• 1616787-09-7 1,5-bis(2,5-dimethylthiophen-3-yl)-3-(4-nitrophenyl)pentane-1,5-dione 
• 1616787-12-2 C₃₅H₃₁NS₄ 
• 1312809-18-9 1-[4-[4-(2-methoxyphenyl)piperazin-1-yl]butyl]-4-(4-nitrophenyl)piperidine-2,6-dione 
• 1312809-17-8 1-[3-[4-(2-methoxyphenyl)piperazin-1-yl]propyl]-4-(4-nitrophenyl)piperidine-2,6-dione 
• 1312809-00-9 1-(4-chlorobutyl)-4-(4-nitrophenyl)piperidine-2,6-dione 
• 1312808-99-3 1-(3-chloropropyl)-4-(4-nitrophenyl)piperidine-2,6-dione 
• 120066-99-1 3-(4-amino-phenyl)-glutaric acid 
• 53911-69-6 3-(4-nitro-phenyl)-pentanedioic acid anhydride 

Relevant articles and documents

Design, synthesis, photochromism and electrochemistry of a novel material with pendant photochromic units

In the present work, the synthesis, photochromism and electrochemistry of a novel material 1, 1-(4-[3,4-bis(2,5-dimethyl-3-thienyl)cyclopent-3-en-1-yl]phenyl)-2,5-di-2-thienyl-1H-pyrrole, with pendant dithienylethene (DTE) photochromic units are described. It should be noted that the system 1 can be reversibly and efficiently switched between open (1o) and closed (1c) states by light in both solution and in the solid poly(methyl methacrylate) matrix. It is also noteworthy that the two isomers (1o and 1c) of this novel system 1 can be smoothly polymerized on ITO by electrochemical means. Surprisingly, the DTE unit in 1 does not retain its photochemical switching properties after immobilization onto ITO. The morphology of the polymer film was investigated by AFM analysis. Furthermore, it was found that the polymer exhibited remarkable electrochromic features that can be switched from green in the neutral state to violet state under applied external potentials without disturbing the photochromic units.

Reducing ion channel activity in a series of 4-heterocyclic arylamide FMS inhibitors

During efforts to improve the bioavailability of FMS kinase inhibitors 1 and 2, a series of saturated and aromatic 4-heterocycles of reduced basicity were prepared and evaluated in an attempt to also improve the cardiovascular safety profile over lead ary

Three multicomponent reactions of 3,5-dimethyl-4-nitroisoxazole

The title compound is used to prepare 3-arylglutaric acids, bis-isoxazoles and bis-pyrazoles from commercially available materials. The methodologies described have afforded important synthetic intermediates in high yields and without the use of chromatography.