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[4-[2-(4-Fluorophenyl)vinyl]phenyl]diphenylamine is a chemical compound with the molecular formula C30H23FN. It is a derivative of diphenylamine and belongs to the class of organic compounds known as diphenylamines. [4-[2-(4-Fluorophenyl)vinyl]phenyl]diphenylamine possesses a conjugated structure and electronic properties that make it suitable for various applications.

666830-53-1

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666830-53-1 Usage

Uses

Used in Rubber and Lubricant Industry:
[4-[2-(4-Fluorophenyl)vinyl]phenyl]diphenylamine is used as an antioxidant and stabilizer for enhancing the durability and performance of rubber and lubricants. It functions as a free radical scavenger, preventing degradation and oxidation of these materials, thereby extending their service life and improving their overall quality.
Used in Organic Electronics and Optoelectronics:
Due to its conjugated structure and electronic properties, [4-[2-(4-Fluorophenyl)vinyl]phenyl]diphenylamine has potential applications in the field of organic electronics and optoelectronics. It can be utilized in the development of electronic devices and components that require specific electronic characteristics, such as conductivity and light emission.

Check Digit Verification of cas no

The CAS Registry Mumber 666830-53-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,6,8,3 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 666830-53:
(8*6)+(7*6)+(6*6)+(5*8)+(4*3)+(3*0)+(2*5)+(1*3)=191
191 % 10 = 1
So 666830-53-1 is a valid CAS Registry Number.

666830-53-1Downstream Products

666830-53-1Relevant academic research and scientific papers

Spectroscopic Correlations between Supermolecules and Molecules. Anatomy of the Ion-Modulated Electronic Properties of the Nitrogen Donor in Monoazacrown-Derived Intrinsic Fluoroionophores

Yang, Jye-Shane,Hwang, Chung-Yu,Hsieh, Chia-Chun,Chiou, Shih-Yi

, p. 719 - 726 (2004)

The synthesis, absorption and emission spectra, fluorescence quantum yields, and fluorescence lifetimes of three compound series of trans-4,4′-disubstituted aminostilbenes (1-3) are reported. The chromo-/fluoroionophoric behavior of the monoaza-15-crown-5

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