Welcome to LookChem.com Sign In|Join Free
  • or
5,8-DICHLORO-4-HYDROXYQUINOLINE, also known as oxolinic acid, is a synthetic quinolone antibiotic with potent antibacterial and antifungal properties. It is effective in inhibiting the synthesis of bacterial DNA, particularly against Gram-negative organisms, and is commonly used in veterinary medicine for treating urinary tract and respiratory infections in animals.

53790-82-2

Post Buying Request

53790-82-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

53790-82-2 Usage

Uses

Used in Veterinary Medicine:
5,8-DICHLORO-4-HYDROXYQUINOLINE is used as an antibacterial and antifungal agent for treating various infections in animals, particularly urinary tract and respiratory infections. Its effectiveness in inhibiting bacterial DNA synthesis makes it a valuable asset in veterinary medicine.
Used in Antimicrobial Research:
5,8-DICHLORO-4-HYDROXYQUINOLINE is used as a subject of study for its antimicrobial properties and potential therapeutic applications. Extensive research has been conducted to understand its mechanism of action, effectiveness against different types of bacteria, and possible synergistic effects with other antibiotics.
Used in Drug Development:
5,8-DICHLORO-4-HYDROXYQUINOLINE serves as a starting point for the development of new antimicrobial drugs. Its unique structure and activity against specific bacterial strains provide a foundation for designing more effective and targeted treatments for various infections.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5,8-DICHLORO-4-HYDROXYQUINOLINE is used as an active pharmaceutical ingredient in the formulation of oral dosage forms, such as tablets and capsules, for the treatment of bacterial infections in animals.
Used in Microbiology Labs:
5,8-DICHLORO-4-HYDROXYQUINOLINE is used as a reference compound in microbiology labs for testing the susceptibility of bacterial strains to quinolone antibiotics. This helps in determining the effectiveness of the compound and its potential use in treating specific infections.

Check Digit Verification of cas no

The CAS Registry Mumber 53790-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,9 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53790-82:
(7*5)+(6*3)+(5*7)+(4*9)+(3*0)+(2*8)+(1*2)=142
142 % 10 = 2
So 53790-82-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H5Cl2NO/c10-5-1-2-6(11)9-8(5)7(13)3-4-12-9/h1-4H,(H,12,13)

53790-82-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,8-dichloro-1H-quinolin-4-one

1.2 Other means of identification

Product number -
Other names 5,8-Dichloro-4-hydroxyquinoline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:53790-82-2 SDS

53790-82-2Relevant academic research and scientific papers

For antibacterial chlorine oxygen kui derivatives

-

, (2017/08/29)

The invention relates to an oxo-quinoline derivative with activity of resisting bacterial infection relevant diseases such as helicobacter pylori (Hp) infection disease. The invention specifically relates to a compound as shown in formula I in the specification, and a pharmaceutically acceptable salt, solvate or prodrug thereof, wherein R is selected from hydrogen, -C alkyl, -C alkenyl, -C alkynyl, or -C alkyl-phenyl, and the alkyl, alkenyl, alkynyl and phenyl can be randomly substituted by halogen, nitro, cyan, hydroxyl, -C alkoxy and phenyl; R is selected from hydrogen, -CONHR and -COOR, R and R are independently selected from -C alkyl and -C alkyl amino, and the amino is randomly substituted by one to two -C alkyls; R is selected from halogen, -C alkoxy, morpholinyl or piperazinyl.

With anti-tumor activity of chlorine oxygen kui derivatives

-

Paragraph 0319; 0320; 0321, (2017/12/28)

The invention relates to a chloroxoquinoline derivatives with anti-tumor activity and specifically relates to compounds of a formula I as shown in the specification and pharmaceutically acceptable salts, solvates and prodrugs thereof, wherein R1 is selected from hydrogen, -C1-6 alkyl, -C2-6 alkenyl, -C2-6 alkynyl and -C1-6 alkyl-phenyl, and the alkyl, the alkenyl, the alkynyl and the phenyl can be optionally substituted by halogens, nitryl, cyan, hydroxyl, -C1-6 alkoxy and phenyl; R3 is selected from hydrogen, -CONHR31 and -COOR32, the R31 and the R32 are independently selected from -C1-6 alkyl and -C1-6 alkylamino, respectively, and the amino can be optionally substituted by 1 to 2 -C1-6 alkyls; R7 is selected from halogens, -C1-6 alkoxy, morpholinyl and piperazine; the formula I is as shown in the specification.

Synthesis of novel halogenated 4(1H)-quinolones by thermolysis of arylaminomethylene-1,3-dioxane-4,6-diones

Rotzoll, Sven,Reinke, Helmut,Fischer, Christine,Langer, Peter

experimental part, p. 69 - 78 (2009/06/17)

A variety of novel 4(1H)-quinolone derivatives were prepared by thermolysis of aminomethylene Meldrum's acid derivatives. Georg Thieme Verlag Stuttgart.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 53790-82-2