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1,2,8-TRIHYDROXYANTHRAQUINONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51030-24-1

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51030-24-1 Usage

Class

Anthraquinone derivatives

Color

Red-brown

Industry use

Dye industry

Application

pH indicator

Application

Synthesis of various dyes

Application

Key intermediate in the production of pharmaceuticals and agrochemicals

Potential properties

Antioxidant

Potential properties

Anti-inflammatory

Fields of interest

Medicine and biochemistry

Versatility

Wide range of applications in different industries

Check Digit Verification of cas no

The CAS Registry Mumber 51030-24-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,3 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51030-24:
(7*5)+(6*1)+(5*0)+(4*3)+(3*0)+(2*2)+(1*4)=61
61 % 10 = 1
So 51030-24-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H8O5/c15-8-3-1-2-6-10(8)14(19)11-7(12(6)17)4-5-9(16)13(11)18/h1-5,15-16,18H

51030-24-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,8-trihydroxyanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 1,2,8-trihydroxy-9,10-anthracenedione

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:51030-24-1 SDS

51030-24-1Downstream Products

51030-24-1Relevant academic research and scientific papers

Novel anthraquinones and process for the preparation and method of use thereof

-

Page/Page column 3; 5; figure 2, (2008/06/13)

A process for the preparation of hydroxyl substituted anthraquinones is described. The process couples a phthalic anhydride (substituted or unsubstituted) to benzene ring moiety substituted with at least two hydroxyl groups. Remaining hydroxy groups were converted to methoxy groups in some anthraquinones. The compounds are particularly useful for the treatment of parasitic diseases. Also, a method of treating or preventing malaria, filariasis schistosomiasis and other parasitic diseases using anthraquinones.

Synthesis and activity of substituted anthraquinones against a human filarial parasite, Brugia malayi

Dhananjeyan, Mugunthu R.,Milev, Youli P.,Kron, Michael A.,Nair, Muraleedharan G.

, p. 2822 - 2830 (2007/10/03)

Lymphatic filariasis (elephantiasis) is a global public health problem caused by the parasitic nematodes Wuchereria bancrofti and Brugia malayi. We have previously reported anthraquinones from daylily roots with potent activity against pathogenic trematode Schistosoma mansoni. Here we report the synthesis of novel anthraquinones A-S and their antifilrarial activity. Anthraquinones A-S were synthesized by a single-step Friedel-Crafts acylation reaction between phthalic anhydrides and substituted benzenes. The antifilarial properties of these synthetic anthraquinones were tested against microfilaria as well as adult male and female worms of B. malayi. The most active anthraquinone was K, which showed 100% mortality within 1, 5, and 3 days, respectively, against microfilaria and adult male and female worms at 5 ppm concentration. Albendazole, an oral drug currently used to treat parasitic infections, was used as a positive control. Methylated products of anthraquinones did not affect the microfilaria. Histological examination of treated adult female parasites showed most of the anthraquinones caused marked effects on intrauterine embryos.

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