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Dysprosium chloride is a chemical compound consisting of dysprosium and chlorine, characterized by its pale green solid appearance and high solubility in water. It is a versatile compound with distinctive magnetic and luminescent properties, playing a significant role in various advanced technologies.

10075-74-8

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10075-74-8 Usage

Uses

Used in Permanent Magnets Industry:
Dysprosium chloride serves as a precursor for the production of dysprosium metal, which is extensively used in the manufacturing of high-performance permanent magnets. These magnets are crucial for various applications, including electric vehicles, wind turbines, and consumer electronics, due to their superior magnetic properties.
Used in Lighting Industry:
Dysprosium chloride contributes to the production of dysprosium metal, which is utilized in lighting technologies, particularly in phosphors for white LED lights. The incorporation of dysprosium enhances the light output and energy efficiency, making it an essential component in modern lighting solutions.
Used in Technological Devices:
Dysprosium chloride is employed in the synthesis of various technological devices, such as sensors, actuators, and optical components, owing to the unique properties of dysprosium metal. Its magnetic and luminescent characteristics make it a valuable material in the development of innovative technologies.
Used in Specialty Glasses and Ceramics Industry:
Dysprosium chloride is used in the production of specialty glasses and ceramics, where it imparts specific optical, mechanical, and thermal properties. These materials are employed in high-temperature applications, such as aerospace components and advanced electronics, benefiting from the exceptional characteristics of dysprosium.
Used in Chemical Catalysts Synthesis:
Dysprosium chloride plays a role in the synthesis of chemical catalysts, which are essential in various chemical reactions and industrial processes. The unique properties of dysprosium enable the development of efficient and selective catalysts, contributing to advancements in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 10075-74-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,7 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10075-74:
(7*1)+(6*0)+(5*0)+(4*7)+(3*5)+(2*7)+(1*4)=68
68 % 10 = 8
So 10075-74-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H12S2/c1-13-11-7-3-6-10-9(11)5-4-8-12(10)14-2/h3-8H,1-2H3

10075-74-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5-bis(methylsulfanyl)naphthalene

1.2 Other means of identification

Product number -
Other names 1,5-Bis-methylthio-naphthalin

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:10075-74-8 SDS

10075-74-8Downstream Products

10075-74-8Relevant articles and documents

ORGANIC PHOTOELECTRIC CONVERSION ELEMENT

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Paragraph 0073; 0076, (2020/06/15)

A photoelectric conversion element uses organic materials and is provided with improved quantum efficiency and response rate. The organic photoelectric conversion element includes, in a photoelectric conversion layer, p-type molecules represented by Formu

Thioether-Directed Peri-Selective C-H Arylation under Rhodium Catalysis: Synthesis of Arene-Fused Thioxanthenes

Moon, Sanghun,Nishii, Yuji,Miura, Masahiro

supporting information, p. 233 - 236 (2019/01/10)

A rhodium-catalyzed direct C-H arylation of naphthalene and anthracene was developed with the assistance of a thioether directing group. The reaction proceeded with exclusive peri-selectivity, and the series of coupling products were readily transformed i

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