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55764-56-2

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55764-56-2 Usage

General Description

6-nitro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid is a chemical compound that belongs to the quinoline carboxylic acid group. It is a yellow crystalline solid that is insoluble in water but soluble in organic solvents. 6-nitro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid is commonly used in the synthesis of pharmaceuticals and agrochemicals due to its structural versatility and biological activity. It has been studied for its antimicrobial and antitumor properties, making it a potential candidate for drug development. Additionally, it has been found to exhibit antioxidant and anti-inflammatory activities, making it a versatile compound with potential uses in a variety of fields.

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

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Buechi et al.

, p. 858,862 (1950)

-

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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