92289-14-0

Usage

Uses

Used in Organic Synthesis:
3-(4-nitrophenyl)pentanedioic acid serves as a key intermediate in the synthesis of complex organic molecules, contributing to the development of novel chemical entities with potential applications in various fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3-(4-nitrophenyl)pentanedioic acid is utilized as a building block for the design and synthesis of new drug candidates. Its unique structural features allow for the exploration of its therapeutic potential in treating various diseases and conditions.
Used in Coordination Chemistry:
3-(4-nitrophenyl)pentanedioic acid is employed in coordination chemistry due to its ability to form stable complexes with metal ions. This property is valuable for the development of new materials with specific catalytic, electronic, or magnetic properties.
Used in Analytical Chemistry:
As a reagent in analytical chemistry, 3-(4-nitrophenyl)pentanedioic acid is particularly useful for the determination of metal ions in solution. Its affinity for metal ions aids in the accurate quantification and analysis of these elements in various samples.

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

• 64-17-5 ethanol 
• 53911-69-6 3-(4-nitro-phenyl)-pentanedioic acid anhydride 
• 7647-01-0 hydrogenchloride 
• 126989-14-8 tetraethyl 2-(4-nitrophenyl)propane-1,1,3,3-tetracarboxylate 
• 93711-15-0 5-hydroxy-5-methyl-3-(4-nitrophenyl)cyclohexanone-2,4-dicarboxylic acid diethyl ester 
• 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 

Downstream Products

• 53911-69-6 3-(4-nitro-phenyl)-pentanedioic acid anhydride 
• 120066-99-1 3-(4-amino-phenyl)-glutaric acid 
• 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 

Relevant academic research and scientific papers

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.

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

INHIBITORS OF C-FMS KINASE

The invention is directed to compounds of Formula I: wherein Z, X, J, R2 and W are set forth in the specification, as well as solvates, hydrates, tautomers and pharmaceutically acceptable salts thereof, that inhibit protein tyrosine kinases, es

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.