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2051-10-7

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2051-10-7 Usage

Description

5,6-CHRYSENEQUINONE is a polycyclic aromatic hydrocarbon quinones, which is a type of organic compound consisting of multiple fused aromatic rings. It has been studied as a possible carcinogen due to its potential harmful effects on human health.

Uses

Used in Organic Chemistry:
5,6-CHRYSENEQUINONE is used as a reactant in various organic reactions for the synthesis of different compounds. Its unique structure and reactivity make it a valuable intermediate in the preparation of various organic molecules.
Used in Research and Development:
Due to its potential carcinogenic properties, 5,6-CHRYSENEQUINONE is used in research and development to study the effects of polycyclic aromatic hydrocarbon quinones on human health and the environment. This helps in understanding the mechanisms of carcinogenesis and developing strategies to mitigate the risks associated with exposure to these compounds.
Used in Environmental Monitoring:
5,6-CHRYSENEQUINONE is also used in environmental monitoring to detect and quantify the presence of polycyclic aromatic hydrocarbon quinones in air, water, and soil samples. This helps in assessing the level of pollution and taking necessary measures to control the release of these harmful compounds into the environment.
Used in Pharmaceutical Industry:
Although 5,6-CHRYSENEQUINONE is a potential carcinogen, its unique chemical properties may be exploited in the development of new drugs or drug candidates. Researchers in the pharmaceutical industry may use it as a starting material or a structural motif in the design of novel therapeutic agents.
Used in Material Science:
The electronic and optical properties of 5,6-CHRYSENEQUINONE make it a potential candidate for use in the development of advanced materials, such as organic semiconductors or photovoltaic devices. Researchers in material science may explore its potential applications in these fields to create innovative technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 2051-10-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2051-10:
(6*2)+(5*0)+(4*5)+(3*1)+(2*1)+(1*0)=37
37 % 10 = 7
So 2051-10-7 is a valid CAS Registry Number.
InChI:InChI=1/C18H10O2/c19-17-15-8-4-3-7-13(15)14-10-9-11-5-1-2-6-12(11)16(14)18(17)20/h1-10H

2051-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name chrysene-5,6-dione

1.2 Other means of identification

Product number -
Other names Chrysene-5,6-quinone

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:2051-10-7 SDS

2051-10-7Relevant articles and documents

Ruthenium nanoparticles supported on mesoporous MCM-41 as an efficient and reusable catalyst for selective oxidation of arenes under ultrasound irradiation

Khorshidi, Alireza

, p. 153 - 158 (2016/01/12)

Mesoporous MCM-41 was used as a support for the uniform dispersion of ruthenium nanoparticles having an average particle size of ~5 nm. The obtained nanocomposite, MCM-41-Ru, was characterized using inductively coupled plasma, transmission electron microscopy, energy dispersive X-ray analysis, X-ray diffraction, and BET surface area measurements. The material was employed as an efficient and recyclable catalyst in the ultrasound-assisted oxidation of arenes. It was observed that ultrasound irradiation in combination with KBrO3 as the oxidant, in the presence of MCM-41-Ru nanoparticles, accelerates the oxidation reaction to afford the desired products in good yields. The recovered catalyst retained activity for successive runs, with a continuous change in the nature of its active sites.

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