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5,8-Dihydro-4,6-dihydroxy-5,8-dioxo-2-quinolinecarboxylic acid is a quinolinecarboxylic acid derivative with the molecular formula C11H7NO6. It features two hydroxyl groups and two carbonyl groups, and exhibits potential biological activity. This chemical compound is utilized in the synthesis of pharmaceuticals, particularly for the development of anti-microbial, anti-inflammatory, and anti-cancer drugs. It is also being studied for its antioxidant properties and its ability to inhibit the growth of certain bacteria and fungi.

98948-82-4

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98948-82-4 Usage

Uses

Used in Pharmaceutical Industry:
5,8-Dihydro-4,6-dihydroxy-5,8-dioxo-2-quinolinecarboxylic acid is used as an intermediate in the synthesis of various pharmaceuticals for its potential biological activity. It plays a crucial role in the development of anti-microbial, anti-inflammatory, and anti-cancer drugs, contributing to the creation of novel treatments for a range of diseases and conditions.
Used in Antimicrobial Applications:
In the field of antimicrobial research, 5,8-Dihydro-4,6-dihydroxy-5,8-dioxo-2-quinolinecarboxylic acid is used as a compound with potential to inhibit the growth of certain bacteria and fungi. Its ability to interfere with microbial processes makes it a valuable asset in the development of new antimicrobial agents.
Used in Antioxidant Research:
5,8-Dihydro-4,6-dihydroxy-5,8-dioxo-2-quinolinecarboxylic acid is also used as a subject of study in antioxidant research. Its potential antioxidant properties are of interest to scientists who are looking for new ways to combat oxidative stress and related conditions.
Used in Anti-inflammatory Applications:
As an anti-inflammatory agent, 5,8-Dihydro-4,6-dihydroxy-5,8-dioxo-2-quinolinecarboxylic acid is used in the development of medications aimed at reducing inflammation. Its potential to alleviate inflammation can be harnessed to improve the treatment of various inflammatory diseases.
Used in Anticancer Drug Development:
In oncology, 5,8-Dihydro-4,6-dihydroxy-5,8-dioxo-2-quinolinecarboxylic acid is used as a key component in the development of anti-cancer drugs. Its role in creating pharmaceuticals that target cancer cells is vital for advancing cancer treatment options and improving patient outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 98948-82-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,9,4 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 98948-82:
(7*9)+(6*8)+(5*9)+(4*4)+(3*8)+(2*8)+(1*2)=214
214 % 10 = 4
So 98948-82-4 is a valid CAS Registry Number.

98948-82-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-hydroxy-4,5,6-trioxo-1H-quinoline-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4,6-Dihydroxy-chinolinchinon-(5,8)-carbonsaeure-(2)

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:98948-82-4 SDS

98948-82-4Downstream Products

98948-82-4Relevant academic research and scientific papers

A synthesis method for 4,6-dihydroxy quinoline-5,8-diquinone-2-formic acid medicine intermediate

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Paragraph 0014-0025, (2018/09/08)

The invention discloses a synthesis method for 4,6-dihydroxy quinoline-5,8-diquinone-2-formic acid medicine intermediate including the following steps: adding 4,6-dihydroxy-5,8-dimethoxy-quinoline-2-formic acid and an octane solution into a reaction container, raising the temperature, adding potassium persulfate in batches, controlling the stirring speed, adding an aqueous solution, and continuingthe reaction; adding cadmium nitrate powder, rising the solution temperature, adding potassium sulfate solution, continuing the reaction, reducing the temperature, standing, allowing layering of thesolution, adding a sodium chloride solution to wash multiple times and adding a methyl ether solution to wash multiple times, recrystallizing in an o-chlorotoluene solution, performing dehydration with a dehydrating agent, and obtaining the finished product of the 4,6-dihydroxy quinoline-5,8-diquinone-2-formic acid.

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