40915-22-8 Usage
Uses
Used in Polymer Production:
4,4-Diiododiphenylsulfone is used as a building block in the synthesis of high-performance polymers, such as poly(aryl ether sulfone) and poly(aryl ether ketone). These polymers are known for their exceptional thermal stability and chemical resistance, making them ideal for applications in various industries.
Used in Aerospace Industry:
In the aerospace industry, 4,4-Diiododiphenylsulfone is used in the production of polymers that are employed in the manufacturing of aircraft components. The high thermal stability and chemical resistance of these polymers contribute to the overall performance and durability of the aircraft.
Used in Automotive Industry:
4,4-Diiododiphenylsulfone is utilized in the automotive industry for the production of polymers that are used in the manufacturing of various automotive components. These polymers offer enhanced thermal stability and chemical resistance, ensuring the longevity and reliability of the components.
Used in Electronics Industry:
In the electronics industry, 4,4-Diiododiphenylsulfone is used in the synthesis of polymers that are employed in the production of electronic devices and components. The high thermal stability and chemical resistance of these polymers help protect the devices from harsh environmental conditions and ensure their proper functioning.
Used in Medical and Healthcare Applications:
4,4-Diiododiphenylsulfone is known to possess antibacterial and antifungal properties, making it potentially valuable in medical and healthcare applications. Its ability to inhibit the growth of harmful microorganisms can contribute to the development of new materials and products for use in healthcare settings.
However, it is important to consider the toxicity and environmental impact of 4,4-Diiododiphenylsulfone when handling and disposing of this chemical. Proper safety measures and disposal methods should be implemented to minimize any potential risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 40915-22-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,1 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40915-22:
(7*4)+(6*0)+(5*9)+(4*1)+(3*5)+(2*2)+(1*2)=98
98 % 10 = 8
So 40915-22-8 is a valid CAS Registry Number.
40915-22-8Relevant academic research and scientific papers
Organic light-emitting material with room-temperature phosphorescence performance and preparation method and application thereof
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Paragraph 0049-0052, (2021/05/29)
The invention discloses an organic light-emitting material with room-temperature phosphorescence performance and a preparation method and application thereof, and belongs to the technical field of organic light-emitting materials. The organic light-emitti
Synthesis of symmetrical diaryl sulfone by homocoupling of sodium arylsulfinate
Peng, Yao
, p. 265 - 268 (2014/06/09)
An efficient practical homocoupling reaction of sodium arylsulfinate promoted by Cu(II) is reported whereby symmetrical diaryl sulfone derivatives are obtained with high selectivity and reactivity by intermolecular cross-coupling. This homocoupling reacti
Process for preparing halo-substituted diarylsulfones
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, (2008/06/13)
A process for preparing diarylsulfone, the process comprising reacting chlorosulfonic acid with a mixture of (i) aromatic hydrocarbon represented by the formula STR1 wherein one of X and Y is a halogen atom and the other is a halogen atom or a hydrogen atom and (ii) aromatic sulfonic acid represented by the formula STR2 wherein X and Y are as defined above.
