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Quinoline-5,6-dione, also known as 5,6-dihydroxyquinoline-2-carboxylic acid or 5,6-dihydroxy-2-quinolone, is an organic compound with the molecular formula C9H5NO3. It is a derivative of quinoline, a heterocyclic aromatic compound consisting of a benzene ring fused to a pyridine ring. Quinoline-5,6-dione is characterized by the presence of two hydroxyl groups at the 5 and 6 positions and a carbonyl group at the 2 position. quinoline-5,6-dione is of interest in various fields, including pharmaceuticals and materials science, due to its potential applications in the synthesis of drugs, dyes, and other organic compounds. It can be synthesized through various methods, such as oxidation of quinoline derivatives or condensation reactions, and is often used as a building block for more complex molecules.

7467-33-6

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7467-33-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7467-33-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7467-33:
(6*7)+(5*4)+(4*6)+(3*7)+(2*3)+(1*3)=116
116 % 10 = 6
So 7467-33-6 is a valid CAS Registry Number.

7467-33-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name quinoline-5,6-dione

1.2 Other means of identification

Product number -
Other names Chinolin-5,6-dion

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:7467-33-6 SDS

7467-33-6Downstream Products

7467-33-6Relevant academic research and scientific papers

Room temperature stable multitalent: highly reactive and versatile copper guanidine complexes in oxygenation reactions

Paul, Melanie,Hoffmann, Alexander,Herres-Pawlis, Sonja

, p. 249 - 263 (2021/02/26)

Inspired by the efficiency of natural enzymes in organic transformation reactions, the development of synthetic catalysts for oxygenation and oxidation reactions under mild conditions still remains challenging. Tyrosinases serve as archetype when it comes to hydroxylation reactions involving molecular oxygen. We herein present new copper(I) guanidine halide complexes, capable of the activation of molecular oxygen at room temperature. The formation of the reactive bis(μ-oxido) dicopper(III) species and the influence of the anion are investigated by UV/Vis spectroscopy, mass spectrometry, and density functional theory. We highlight the catalytic hydroxylation activity towards diverse polycyclic aromatic alcohols under mild reaction conditions. The selective formation of reactive quinones provides a promising tool to design phenazine derivatives for medical applications. Graphic abstract: [Figure not available: see fulltext.]

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