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2207-41-2

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2207-41-2 Usage

General Description

9-Acridanone, 10-ethyl- is a chemical compound with the molecular formula C15H13NO. It is a derivative of acridine and is used primarily as an intermediate in the manufacture of various pharmaceuticals and organic compounds. 9-Acridanone, 10-ethyl- has been studied for its potential antitumor and antiviral activities, and it has also shown to have antioxidant and neuroprotective properties. Additionally, it has been used as a fluorescent dye for biological and chemical research. While it is considered to have low toxicity, further research is needed to fully understand its potential uses and effects.

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 articles and documents

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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