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78846-44-3

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78846-44-3 Usage

Chemical class

Anthracene derivatives

Explanation

1,4-dimethoxyanthracene-9,10-diol belongs to the class of anthracene derivatives, which are aromatic hydrocarbons composed of three benzene rings fused together.

Explanation

This is an alternative name for 1,4-dimethoxyanthracene-9,10-diol, which is used to describe its chemical structure.

Explanation

The compound is used in the production of dyes and pigments, as well as in organic synthesis due to its unique chemical structure.

Explanation

The compound has two methoxy (CH3O) groups attached to the 1 and 4 positions of the anthracene ring, which contribute to its chemical properties.

Explanation

The compound also has two hydroxyl (OH) groups attached to the 9 and 10 positions, which play a role in its colorant and antioxidant properties.

Explanation

The chemical structure of 1,4-dimethoxyanthracene-9,10-diol, with its methoxy and hydroxyl groups, makes it particularly useful for its colorant properties, which is why it is used in the production of dyes and pigments.

Explanation

The molecular formula of 1,4-dimethoxyanthracene-9,10-diol is C18H16O4, which represents the number of carbon (C), hydrogen (H), and oxygen (O) atoms in the molecule.

Explanation

The molecular weight of 1,4-dimethoxyanthracene-9,10-diol is approximately 296 grams per mole, which is a measure of the mass of one mole of the compound.

Explanation

1,4-dimethoxyanthracene-9,10-diol is a solid at room temperature, which is a common physical state for many organic compounds.

Applications

Dyes and pigments, organic synthesis

Methoxy groups

Two CH3O groups at positions 1 and 4

Hydroxyl groups

Two OH groups at positions 9 and 10

Colorant properties

Useful for creating dyes and pigments

Antioxidant properties

Potential use in pharmaceutical and chemical industries

Molecular weight

Approximately 296 g/mol

Physical state

Solid

Check Digit Verification of cas no

The CAS Registry Mumber 78846-44-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,4 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78846-44:
(7*7)+(6*8)+(5*8)+(4*4)+(3*6)+(2*4)+(1*4)=183
183 % 10 = 3
So 78846-44-3 is a valid CAS Registry Number.

78846-44-3SDS

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-dimethoxyanthracene-9,10-diol

1.2 Other means of identification

Product number -
Other names 1,4-Dimethoxy-9,10-dihydroxy-anthracen

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:78846-44-3 SDS

78846-44-3Upstream product

78846-44-3Relevant articles and documents

Experiments Directed Towards the Synthesis of Anthracyclinones. XIX. Elaboration of 2-Formylquinizarin Through a Wittig Reaction

Boniface, Peter J.,Cambie, Richard C.,Carroll, David R.,Marsh, Nicholas F.,Milbank, Jared B. J.,et al.

, p. 441 - 450 (2007/10/02)

Reaction of 2-formylquinizarin dimethyl ether (3) with the dimethoxy ylide (6) gives an α,β-unsaturated ester (8) which on hydrogenation, reduction and methylation gives the tetramethoxyanthracene diester (18).When linked to work by Doetz and Popall this

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