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α-Deuteriobenzyl phenyl ketone is a deuterated derivative of benzyl phenyl ketone, a chemical compound with the molecular formula C13H11DO. It is characterized by the presence of a deuterium atom (D) at the α-carbon position, which is adjacent to the carbonyl group. This deuterium substitution can significantly affect the compound's chemical reactivity and physical properties, such as its boiling point and solubility. α-Deuteriobenzyl phenyl ketone is often used in organic synthesis, particularly in reactions where the deuterium isotope effect is of interest, such as in kinetic isotope effects studies or in the synthesis of isotopically labeled compounds for various applications, including pharmaceuticals and materials science.

84369-12-0

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84369-12-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84369-12-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,3,6 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 84369-12:
(7*8)+(6*4)+(5*3)+(4*6)+(3*9)+(2*1)+(1*2)=150
150 % 10 = 0
So 84369-12-0 is a valid CAS Registry Number.

84369-12-0Downstream Products

84369-12-0Relevant academic research and scientific papers

Photocatalytic Coproduction of Deoxybenzoin and H2 through Tandem Redox Reactions

Luo, Nengchao,Hou, Tingting,Liu, Shiyang,Zeng, Bin,Lu, Jianmin,Zhang, Jian,Li, Hongji,Wang, Feng

, p. 762 - 769 (2020/01/02)

Photocatalytic H2 evolution from organic feedstocks with simultaneous utilization of photogenerated holes achieves solar energy storage and coproduces value-Added chemicals. Here we show visible-light H2 production from benzyl alcohol (BAL) with controllable generation of deoxybenzoin (DOB) or benzoin (BZ) through tandem redox reactions. Particularly, DOB synthesis circumvents the use of expensive feedstocks and environmentally unfriendly catalysts that are required previously. Under the irradiation of blue LEDs, the key of steering the major product to DOB rather than BZ is to decrease the conduction band bottom potentials of the ZnIn sulfide catalysts by increasing the Zn/In ratio, which results in the dehydration of intermediate hydrobenzoin (HB) to DOB proceeding in a redox-neutral mechanism and consuming an electron-hole pair. As a proof of concept, this method is used to synthesize DOB derivatives in gram scale.

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