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6486-93-7

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6486-93-7 Usage

Preparation

(a) in the presence of ?Boric acid, with fuming sulfuric acid oxidation 1,2-Dihydroxyanthracene-9,10-dione , and hydrolysis; (b) 5,6-Dihydroxy-9,10-dioxo-9,10-dihydroanthracene-1-sulfonic acid?and sodium hydroxide reaction; (c) 1,5-Dihydroxyanthracene-9,10-dione with Sodium nitrate and Sodium hydroxide or had better use Sodium hydroxide and Potassium hydroxide mixture for oxidation.

Properties and Applications

bordeaux (aluminum), dark purplish red (chromium). Soluble in ethanol and Acetic acid glacial. In concentrated sulfuric acid to dark purple, dilution after yellow orange precipitation; In concentrated sulfuric acid Boric acid added to blue. Standard(cotton) Ironing Fastness Light Fastness Fulling Persperation Fastness Soaping Water Alkali Acid ISO 6 5

Alkali

Acid

Check Digit Verification of cas no

The CAS Registry Mumber 6486-93-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,8 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6486-93:
(6*6)+(5*4)+(4*8)+(3*6)+(2*9)+(1*3)=127
127 % 10 = 7
So 6486-93-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H8O5/c15-8-3-1-2-6-10(8)12(17)7-4-5-9(16)14(19)11(7)13(6)18/h1-5,15-16,19H

6486-93-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,5-trihydroxyanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 1,2,5-Trihydroxy-anthrachinon

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:6486-93-7 SDS

6486-93-7Relevant articles and documents

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

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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.

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