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1-hydroxyanthrone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1715-81-7

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1715-81-7 Usage

Safety Profile

Questionable carcinogen withexperimental neoplastigenic data. When heated todecomposition it emits acrid smoke and irritating fumes.

Check Digit Verification of cas no

The CAS Registry Mumber 1715-81-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,1 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1715-81:
(6*1)+(5*7)+(4*1)+(3*5)+(2*8)+(1*1)=77
77 % 10 = 7
So 1715-81-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H10O2/c15-12-7-3-5-10-8-9-4-1-2-6-11(9)14(16)13(10)12/h1-7,15H,8H2

1715-81-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroxy-10H-anthracen-9-one

1.2 Other means of identification

Product number -
Other names 1-Hydroxy-9-anthrone

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:1715-81-7 SDS

1715-81-7Downstream Products

1715-81-7Relevant academic research and scientific papers

Easy access to pyranoacridines, pyranoxanthenes, and arylchromenes through a domino reaction

Commandeur, Claude,Florent, Jean-Claude,Rousselle, Patricia,Bertounesque, Emmanuel

supporting information; experimental part, p. 1447 - 1451 (2011/04/25)

A series of pyrano[2,3,4-kl]acridines has been synthesized through an unprecedented domino reaction involving1-hydroxy-3-methoxy-10-methylacridone and Grignard reagents. This method has been successfully applied to xanthone, anthracenone, and benzophenone

Reduction of 1-substituted anthraquinones to 1- and 4-substituted anthrones

Loskutov

, p. 341 - 343 (2007/10/03)

The regioselectivity of reduction of 1-substituted anthraquinones to 1 - or 4-substituted anthrones is determined by both the nature of the substituent and the type of the reducing system used.

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