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3,4-diphenyl-2,5-bis-trimethylsilanyl-cyclopenta-2,4-dienone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18754-38-6

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18754-38-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18754-38-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,5 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18754-38:
(7*1)+(6*8)+(5*7)+(4*5)+(3*4)+(2*3)+(1*8)=136
136 % 10 = 6
So 18754-38-6 is a valid CAS Registry Number.

18754-38-6Downstream Products

18754-38-6Relevant academic research and scientific papers

Structure and Reaction Chemistry of Magnesium Organocuprates Derived from Magnesiacyclopentadienes and Copper(I) Salts

Liu, Liang,Wei, Junnian,Chi, Yue,Zhang, Wen-Xiong,Xi, Zhenfeng

, p. 14762 - 14765 (2016)

The chemistry of magnesium organocuprates, including their synthesis, structures, and reactions, remains underexplored. In this work, by taking advantage of the high reactivity and ready availability of magnesiacyclopentadienes, a series of magnesiacyclopentadiene-based organocuprates were synthesized and structurally characterized. A variety of CuX salts (X=Cl, Br, I, or alkynyl) were successfully applied to react with magnesiacyclopentadienes. Besides CuX salts, AgX salts (X=Cl, alkynyl) also undergwent the above reaction to afford the corresponding magnesium organoargentates. Single-crystal X-ray structural analysis and DFT calculations of these butadienyl magnesium organocuprates revealed unique structural characteristics and bonding modes. These results are also very useful to understand the transmetalation process, since the product can be viewed as the resting-state intermediate of a transmetalation reaction between organomagnesium compounds and coinage-metal salts. Preliminary information on the reaction chemistry of these magnesium organocuprates is provided by their reactions with allyl bromide, benzoyl chloride, and CO2.

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