31912-08-0

Usage

Uses

Used in Pharmaceutical Industry:
(2-chloro-6-nitrophenyl)acetic acid is used as an intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into the molecular structure of drugs, enhancing their therapeutic properties.
Used in Agrochemical Industry:
(2-chloro-6-nitrophenyl)acetic acid is used as a building block in the development of agrochemicals, such as herbicides and pesticides, due to its potential to be integrated into the chemical structure of these products, improving their efficacy in agricultural applications.
Used in Dye Industry:
(2-chloro-6-nitrophenyl)acetic acid is used as a chemical intermediate in the production of dyes, contributing to the color and stability of the dyes in various applications.
Used in Antimicrobial Applications:
(2-chloro-6-nitrophenyl)acetic acid is studied for its potential use as an antimicrobial agent, leveraging its chemical properties to inhibit the growth of microorganisms, offering a possible alternative for treating infections.
Used in Anticancer Research:
(2-chloro-6-nitrophenyl)acetic acid is being investigated for its potential as an anticancer agent, exploring its ability to target and affect cancer cells, with the aim of developing new therapeutic approaches for cancer treatment.

Upstream product

• 83-42-1 6-chloro-2-nitrotoluene 
• 3209-22-1 1,2-Dichloro-3-nitrobenzene 
• 105-53-3 diethyl malonate 
• 56433-01-3 2-chloro-6-nitrobenzyl bromide 
• 95-92-1 oxalic acid diethyl ester 
• 36892-19-0 (2-chloro-6-nitro-phenyl)-pyruvic acid 
• 89277-98-5 2-(2-chloro-6-nitrophenyl)acetonitrile 

Downstream Products

• 100376-53-2 2-(2-amino-6-chlorophenyl)ethyl alcohol 
• 102493-68-5 2-(2-chloro-6-nitrophenyl)-ethanol 
• 855423-46-0 4-chloro-3-(4-hydroxy-benzylidene)-indolin-2-one 
• 220327-47-9 3-(4-chloro-2-phenylindol-1-yl)propionic acid 
• 220327-46-8 4-chloro-1-(2-cyanoethyl)-2-phenylindole 
• 220327-49-1 9-Chloro-2-phenyl-4,5-dihydro-pyrrolo[3,2,1-ij]quinolin-6-one 
• 220327-45-7 2-(2-chloro-6-nitrophenyl)acetophenone 
• 66354-66-3 4-chloro-2-phenyl-1H-indole 
• 6127-12-4 (6-Nitro-2-chlor-phenyl)-aceton 
• 119209-28-8 4-(6-Chlor-2-nitrophenyl)acetessigsaeure-ethylester 
• 97522-09-3 methyl 2-(2-chloro-6-nitrophenyl)acetate 

Relevant academic research and scientific papers

Synthesis and diuretic activity of 4,5-dihydro-6H-imidazo[4,5,1- ij]quinoline-6-one 6-oxime-O-sulfonic acid derivatives

Using our previously reported 7-chloro-2,3-dihydro-1-(2-methylbenzoyl)- 4(1H)-quinolinone 4-oxime-O-sulfonic acid potassium salt la (M17055) as a lead, a series of tricyclic (2a-o, 3, 4, 5) and tetracyclic (6) quinolinone oxime O-sulfonic acid derivatives were synthesized by ring annulation of the 1-(2-methylbenzoyl) moiety to the quinolinone skeleton. They were compared with furosemide and compound 1a for diuretic activity in dogs; some tricyclic 4,5-dihydro-6H-imidazo[4,5,1-ij]quinoline-6-one 6-oxime-O-sulfonic acid derivatives showed diuretic activity comparable (2c,e) or superior (2m) to the lead compound 1a. These results are discussed on the basis of a comparison of the conformational and electronic characteristics of the relevant compounds with the aid of computer graphics.

Tricyclic compound or salts thereof, method for producing the same and antimicrobial agent containing the same

A tricyclic compound represented by the general formula (1) and salts thereof. STR1 A method for producing the tricyclic compound and salts thereof, and an antimicrobial agent containing the tricyclic compound and salts thereof as an active ingredient are