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Tris(phenyl-2,4,6-d3)amine, also known as tris(2,4,6-tri-deuteriophenyl)amine, is a deuterated derivative of tris(phenylamine), a common organic compound. tris(phenyl-2,4,6-d3)amine is characterized by three phenyl rings, each substituted with deuterium atoms at the 2, 4, and 6 positions, which replaces the hydrogen atoms in the parent compound. The deuteration can enhance the stability and reduce the volatility of the molecule, making it useful in various applications such as in NMR spectroscopy for studying molecular dynamics and in chemical reactions where isotopic labeling is required. The compound is synthesized by replacing the hydrogen atoms in tris(phenylamine) with deuterium atoms, which can be achieved through chemical reactions involving deuterium gas or deuterated reagents. Tris(phenyl-2,4,6-d3)amine is a valuable tool in research and development, particularly in fields where the study of reaction mechanisms and the effects of isotopic substitution on chemical properties are of interest.

21223-02-9

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21223-02-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21223-02-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,2 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21223-02:
(7*2)+(6*1)+(5*2)+(4*2)+(3*3)+(2*0)+(1*2)=49
49 % 10 = 9
So 21223-02-9 is a valid CAS Registry Number.

21223-02-9Upstream product

21223-02-9Downstream Products

21223-02-9Relevant academic research and scientific papers

B(C6F5)3-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds

Li, Wu,Wang, Ming-Ming,Hu, Yuya,Werner, Thomas

, p. 5768 - 5771 (2017)

Deuterium labeled compounds find widespread application in life science. Herein, the deuteration of electron-rich (hetero)aromatic compounds employing B(C6F5)3 as the catalyst and D2O as the deuterium source is reported. This protocol is highly efficient, simply manipulated, and successfully applied in the deuteration of 23 substrates including natural neurotransmitter-like melatonin. It is assumed that the weakening of the O-D bond ultimately results in the formation of electrophilic D+.

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