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82-35-9

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82-35-9 Usage

Description

1,5-Dinitroanthraquinone, also known as 1,5-Dinitro-9,10-anthraquinone, is an organic compound derived from anthraquinone through nitration. It is characterized by the presence of two nitro groups (-NO2) at the 1 and 5 positions on the anthraquinone molecule. 1 5-DINITROANTHRAQUINONE 97 is known for its unique chemical properties and potential applications in various fields.

Uses

Used in Spectral Flare Compositions:
1,5-Dinitroanthraquinone is used as a component in spectral flare compositions to study the effect of its oxygenous substituents on the color ratio. This application is crucial for understanding the behavior of different chemical compounds when used in pyrotechnic devices, such as flares, which rely on the emission of light through chemical reactions.
Used in the Synthesis of 3,4,7,8-Tetrabromo-1,5-Dinitroanthraquinone:
1,5-Dinitroanthraquinone is used as a starting material to prepare 3,4,7,8-tetrabromo-1,5-dinitroanthraquinone through bromination. This process involves the use of molecular bromine and nitric acid as a co-reagent. The resulting compound, 3,4,7,8-tetrabromo-1,5-dinitroanthraquinone, may have potential applications in various industries, such as the production of dyes, pigments, or other specialty chemicals.
General Description:
1,5-Dinitroanthraquinone is formed as one of the products during the nitration of anthraquinone. This process involves the introduction of nitro groups into the anthraquinone molecule, resulting in the formation of 1,5-dinitroanthraquinone and other isomers, depending on the reaction conditions. The formation of this compound is an important aspect of the chemical synthesis of anthraquinone derivatives, which have a wide range of applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 82-35-9 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82-35:
(4*8)+(3*2)+(2*3)+(1*5)=49
49 % 10 = 9
So 82-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H6N2O6/c17-13-7-3-1-5-9(15(19)20)11(7)14(18)8-4-2-6-10(12(8)13)16(21)22/h1-6H

82-35-9SDS

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 1,5-Dinitroanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 1 5-DINITROANTHRAQUINONE 97

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:82-35-9 SDS

82-35-9Relevant articles and documents

Quinone Compound-Graphene Composite Material, Preparation Method Thereof, and Flexible Lithium Secondary Battery

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Paragraph 0075, (2016/11/07)

A quinone compound-graphene composite material, including quinone compound and graphene, where the quinone compound is chemically bonded on the surface of the graphene, and the quinone compound is quinone compound monomer or quinone polymer. The quinone compound-graphene composite material has high energy density, high flexibility, high conductivity, and high stability, and can be used as cathode material for preparing flexible electrode. Additionally, a preparation method of quinone compound-graphene composite material, and flexible lithium secondary battery uses the quinone compound-graphene composite material as cathode active material.

CONTROLLED NITRATION OF ORGANIC COMPOUNDS. III. POTENTIOMETRIC STUDY OF THE NITRATION OF ANTHRAQUINONE

Kozorez, L. A.,Bondarenko, N. A.

, p. 1854 - 1857 (2007/10/02)

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OXIDATIVE NITRATION OF ANTRAQUINONE AND 2-METHYLANTHRAQUINONE

Ponomarev, V. A.,Esip, V. P.,Yakobi, V. A.

, p. 1682 - 1684 (2007/10/02)

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