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6170-06-5

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6170-06-5 Usage

General Description

Alizarin 1-methyl ether is a chemical compound with the molecular formula C15H12O5. It is a derivative of alizarin, a natural dye found in the roots of the madder plant. Alizarin 1-methyl ether is commonly used as a red dye in the textile industry, and it also has applications in the production of ink, paints, and other colorants. Its chemical structure consists of a core anthraquinone ring with a methyl ether group attached at one of the hydroxyl (OH) positions. This substitution of the hydroxyl group with a methyl ether group alters the chemical properties of alizarin, making it more suitable for certain industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6170-06-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,7 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6170-06:
(6*6)+(5*1)+(4*7)+(3*0)+(2*0)+(1*6)=75
75 % 10 = 5
So 6170-06-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H10O4/c1-19-15-11(16)7-6-10-12(15)14(18)9-5-3-2-4-8(9)13(10)17/h2-7,16H,1H3

6170-06-5SDS

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 2-hydroxy-1-methoxy-9,10-Anthracenedione

1.2 Other means of identification

Product number -
Other names -

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:6170-06-5 SDS

6170-06-5Relevant articles and documents

Synthesis of proposed structure of rennellianone B: A study on rearrangement of anthraquinonyl propargyl ether toward 2H-pyranoanthraquinone

Han, Young Taek

, p. 556 - 558 (2017)

Rennellianone B was originally reported as a natural 2H-pyranoanthraquinone, isolated from the root of Rennellia elliptica Korth. An efficient synthesis of the proposed structure of rennellianone B was accomplished, starting from alizarin. The key feature of the synthesis involves the Claisen rearrangement of the anthraquinonyl propargyl ether intermediate to provide a 2H-pyranoanthraquinone moiety. In addition, intensive studies on rearrangement reaction conditions of anthraquinonyl propargyl ether toward the 2H-pyranoanthraquinone skeleton were described.

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