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15939-83-0

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15939-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15939-83-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,3 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15939-83:
(7*1)+(6*5)+(5*9)+(4*3)+(3*9)+(2*8)+(1*3)=140
140 % 10 = 0
So 15939-83-0 is a valid CAS Registry Number.

15939-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-bis(4-hydroxyanilino)anthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 1,4-bis(4-hydroxyphenylamino)anthraquinone

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:15939-83-0 SDS

15939-83-0Relevant articles and documents

Polymerization of novel methacrylated anthraquinone dyes

Dollendorf, Christian,Kreth, Susanne Katharina,Choi, Soo Whan,Ritter, Helmut

, p. 453 - 459 (2013/04/23)

A new series of polymerizable methacrylated anthraquinone dyes has been synthesized by nucleophilic aromatic substitution reactions and subsequent methacrylation. Thereby, green 5,8-bis(4-(2-methacryloxyethyl)phenylamino)-1,4- dihydroxyanthraquinone (2), blue 1,4-bis(4-((2-methacryloxyethyl)oxy) phenylamino)anthraquinone (6) and red 1-((2-methacryloxy-1,1- dimethylethyl)amino)anthraquinone (12), as well as 1-((1,3-dimethacryloxy-2- methylpropan-2-yl)amino)anthraquinone (15) were obtained. By mixing of these brilliant dyes in different ratios and concentrations, a broad color spectrum can be generated. After methacrylation, the monomeric dyes can be covalently emplaced into several copolymers. Due to two polymerizable functionalities, they can act as cross-linking agents. Thus, diffusion out of the polymer can be avoided, which increases the physiological compatibility and makes the dyes promising compounds for medical applications, such as iris implants.

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