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4-Hydroxy-9(10H)-acridinone, also known as 4-hydroxyacridinone, is a chemical compound with the molecular formula C13H9NO2. It is a derivative of acridinone, a tricyclic aromatic compound with a central nitrogen atom. This white crystalline solid is an important intermediate in the synthesis of various acridine-based compounds, which have applications in pharmaceuticals, dyes, and other chemical industries. 4-Hydroxyacridinone is known for its potential antitumor and antiviral properties, making it a subject of interest in medicinal chemistry research. Its chemical structure features a hydroxyl group attached to the 4-position of the acridinone core, which can participate in various chemical reactions, such as oxidation, reduction, and substitution, to form a range of derivatives with diverse biological activities.

31231-39-7

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31231-39-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31231-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,2,3 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 31231-39:
(7*3)+(6*1)+(5*2)+(4*3)+(3*1)+(2*3)+(1*9)=67
67 % 10 = 7
So 31231-39-7 is a valid CAS Registry Number.

31231-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-9-oxoacridine

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-10H-acridin-9-one

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

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More Details:31231-39-7 SDS

31231-39-7Relevant academic research and scientific papers

Reaction of 4-hydroxyacridin-9(10H)-one and 4-hydroxyacridine-9(10H)-thione with α,ω-alkyl dibromides

Galy, Jean-Pierre,Galy, Anne-Marie,Vichet, Alain,Elguero, Jose

, p. 1199 - 1205 (1998)

Starting from 4-hydroxyacridin-9(10H)-one (1) and 4-hydroxyacridine-9(10H)-thione (2), a series of bis-derivatives was prepared, among them the bridged bis-acridin-(10H)-ones 9-14 and the bis-mercapto-(9H)-acridines 15-18. The reactivity of the 2-and 4-hydroxy series was compared; it was found that it is harder to demethylate 4-methoxy derivatives than their 2-methoxy analogues.

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