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6-nitro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid is a yellow crystalline solid that belongs to the quinoline carboxylic acid group. It is insoluble in water but soluble in organic solvents. This chemical compound is known for its structural versatility and biological activity, making it a promising candidate for various applications.

55764-56-2

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55764-56-2 Usage

Uses

Used in Pharmaceutical Industry:
6-nitro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid is used as an intermediate in the synthesis of pharmaceuticals due to its structural versatility and biological activity. Its antimicrobial and antitumor properties make it a potential candidate for drug development.
Used in Agrochemical Industry:
6-nitro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid is used as a building block in the synthesis of agrochemicals, contributing to the development of new and effective products for agricultural applications.
Used in Antimicrobial Applications:
6-nitro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid is used as an antimicrobial agent, exhibiting activity against various microorganisms. Its potential use in this field can contribute to the development of new antibiotics and antifungal agents.
Used in Antitumor Applications:
6-nitro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid is used as an antitumor agent, showing promise in the development of new cancer treatments. Its potential use in this field can lead to the discovery of novel therapeutic agents for various types of cancer.
Used in Antioxidant and Anti-inflammatory Applications:
6-nitro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid is used as an antioxidant and anti-inflammatory agent, exhibiting potential benefits in various fields, including cosmetics, food industry, and pharmaceuticals. Its versatile properties make it a valuable compound for the development of new products with health-promoting and protective effects.

Check Digit Verification of cas no

The CAS Registry Mumber 55764-56-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,6 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55764-56:
(7*5)+(6*5)+(5*7)+(4*6)+(3*4)+(2*5)+(1*6)=152
152 % 10 = 2
So 55764-56-2 is a valid CAS Registry Number.

55764-56-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-nitro-2-oxo-1H-quinoline-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6-nitro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid

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:55764-56-2 SDS

55764-56-2Relevant articles and documents

Construction and functionalization of fused pyridine ring leading to novel compounds as potential antitubercular agents

Dulla, Balakrishna,Wan, Baojie,Franzblau, Scott G.,Kapavarapu, Ravikumar,Reiser, Oliver,Iqbal, Javed,Pal, Manojit

, p. 4629 - 4635 (2012/07/31)

A series of fused and functionalized pyridine derivatives were designed, synthesized and tested for their potential antitubercular properties. All these novel compounds were prepared by using multistep methods involving the construction of pyridine ring as a key synthetic step. Some of these compounds were found to be interesting when tested for their antitubercular properties in vitro and one of them appeared as an attractive and potential antitubercular agent.

Some Derivatives of Benzazepine. Part III

James, Robert A.,Kohn, Charlotte A.,Rees, Alun H.,Verschuren, Rex E.

, p. 793 - 795 (2007/10/02)

We report the synthesis by two routes, of hitherto unknown 3,4-epoxy-2,3,4,5-tetrahydrobenzazepine-2,5-dione and hence a new route to 2,3,4,5-tetrahydrobenzazepine-2,4,5-triones which are precursors of 2-quinolonecarboxylic acids.

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