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1,5-dihydroxy-4-{[3-(hydroxymethyl)phenyl]amino}-8-nitroanthracene-9,10-dione is a complex organic compound with a molecular formula of C23H17N3O7. It is characterized by the presence of two hydroxyl groups at the 1st and 5th positions, an amino group attached to a 3-(hydroxymethyl)phenyl group at the 4th position, and a nitro group at the 8th position of the anthracene core. The compound also features a 9,10-dione group, indicating the presence of two carbonyl groups at these positions. This chemical is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its unique structure and properties.

3263-48-7

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3263-48-7 Usage

Chemical structure

A complex chemical compound with a central anthracene ring, two hydroxyl groups at positions 1 and 5, a nitro group at position 8, and an amino group attached to a phenyl ring via a methyl group.

Hydroxyl groups

Presence of two hydroxyl groups (-OH) at positions 1 and 5 on the anthracene ring, which can participate in hydrogen bonding and form intermolecular interactions.

Nitro group

A nitro group (-NO2) at position 8 on the anthracene ring, which can impart interesting electronic and redox properties to the compound.

Amino group

An amino group (-NH2) attached to a phenyl ring, which can form hydrogen bonds and participate in various chemical reactions.

Methyl group

A methyl group (-CH3) connecting the phenyl ring to the anthracene structure, which can affect the compound's steric properties and reactivity.

Potential applications

The compound has potential applications in the fields of organic chemistry, material science, pharmaceutical research and development, and chemical reactivity and catalysis studies.

Electronic properties

The presence of nitro and amino groups in the compound can lead to interesting electronic properties, making it a subject of interest for research.

Redox properties

The nitro and amino groups can also impart redox properties to the compound, which can be useful in various chemical reactions and processes.

Chemical reactivity

The unique structure of the compound, including the presence of hydroxyl, nitro, and amino groups, can make it a subject of interest in the study of chemical reactivity and catalysis.

Check Digit Verification of cas no

The CAS Registry Mumber 3263-48-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,6 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3263-48:
(6*3)+(5*2)+(4*6)+(3*3)+(2*4)+(1*8)=77
77 % 10 = 7
So 3263-48-7 is a valid CAS Registry Number.

3263-48-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5-dihydroxy-4-[3-(hydroxymethyl)anilino]-8-nitroanthracene-9,10-dione

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:3263-48-7 SDS

3263-48-7Upstream product

3263-48-7Downstream Products

3263-48-7Relevant academic research and scientific papers

Ethylenically-unsaturated blue anthraquinone dyes

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Page/Page column 4, (2010/02/11)

This invention pertains to certain novel colorant compounds containing one or more ethylenically-unsaturated, photopolymerizable radicals that may be copolymerized (or cured) with ethylenically-unsaturated monomers to produce colored compositions such as colored acrylic polymers. Suitable compositions having the present colorants copolymerized therein include, e.g., polymers produced from acrylate and methacrylate esters, colored polystyrenes, and similar colored polymeric materials derived from other ethylenically-unsaturated monomers. The present invention also pertains to processes for preparing the photopolymerizable colorant compounds. The ethylenically unsaturated colorant compounds may be suitable for use in coatings that are applied to wood, glass, metal, thermoplastics and the like.

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