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9-Acridanone, 10-ethyl-, also known as 10-ethyl-9-acridanone, is a chemical compound with the molecular formula C15H13NO. It is a derivative of acridine, a heterocyclic aromatic compound. 9-Acridanone, 10-ethylhas been studied for its potential applications in pharmaceuticals, organic synthesis, and as a fluorescent dye. It exhibits antitumor, antiviral, antioxidant, and neuroprotective properties, although its low toxicity and further research are required to fully understand its potential uses and effects.

2207-41-2

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2207-41-2 Usage

Uses

Used in Pharmaceutical Industry:
9-Acridanone, 10-ethylis used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique chemical structure and properties make it a valuable building block for the development of new drugs and therapeutic agents.
Used in Antitumor Applications:
9-Acridanone, 10-ethylhas been studied for its potential antitumor activities. It may be employed as an anticancer agent, targeting various types of cancer cells and inhibiting their growth and proliferation. Further research is needed to explore its full potential in this area.
Used in Antiviral Applications:
9-Acridanone, 10-ethylhas also shown potential antiviral activities, making it a candidate for the development of antiviral drugs. It may be used to inhibit the replication and spread of various viruses, providing a new approach to treating viral infections.
Used in Antioxidant Applications:
9-Acridanone, 10-ethylexhibits antioxidant properties, which can be utilized in the development of antioxidants for various applications, including pharmaceuticals, cosmetics, and food preservation. Its ability to neutralize free radicals and protect cells from oxidative damage may contribute to its potential health benefits.
Used in Neuroprotective Applications:
9-Acridanone, 10-ethylhas demonstrated neuroprotective properties, making it a potential candidate for the development of treatments for neurodegenerative diseases such as Alzheimer's, Parkinson's, and Huntington's. Its ability to protect neurons and preserve cognitive function may offer new therapeutic options for these conditions.
Used in Fluorescent Dye Applications:
9-Acridanone, 10-ethylhas been used as a fluorescent dye in biological and chemical research. Its fluorescent properties allow for the visualization and tracking of various biological processes and molecules, contributing to advancements in scientific understanding and discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 2207-41-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2207-41:
(6*2)+(5*2)+(4*0)+(3*7)+(2*4)+(1*1)=52
52 % 10 = 2
So 2207-41-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H13NO/c1-2-16-13-9-5-3-7-11(13)15(17)12-8-4-6-10-14(12)16/h3-10H,2H2,1H3

2207-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-ethylacridin-9-one

1.2 Other means of identification

Product number -
Other names 10-Aethyl-10H-acridin-9-on

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:2207-41-2 SDS

2207-41-2Downstream Products

2207-41-2Relevant academic research and scientific papers

Synergistic effect of ketone and hydroperoxide in Bronsted acid catalyzed oxidative coupling reactions

Schweitzer-Chaput, Bertrand,Sud, Abhishek,Pinter, Aron,Dehn, Stefanie,Schulze, Philipp,Klussmann, Martin

supporting information, p. 13228 - 13232 (2014/01/06)

Waste not wasted: A mechanistic study of the autoxidative coupling of xanthene with cyclopentanone uncovered an autoinductive effect of the waste product hydrogen peroxide. It generates radicals in the presence of acid and ketones, which accelerate the reaction by providing an additional pathway to the reactive hydroperoxide intermediate. This discovery could be applied to achieve other Bronsted acid catalyzed oxidative coupling reactions.

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