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α-Lithium-trimethylsilylmethyldiphenylphosphin is a complex organophosphorus compound with the molecular formula C19H23LiPSi. It is a colorless solid that is highly sensitive to air and moisture, and it is typically stored under an inert atmosphere. α-Lithium-trimethylsilylmethyldiphenylphosphin is characterized by the presence of a lithium atom bonded to a trimethylsilyl group, a methyl group, and a diphenylphosphin group. The diphenylphosphin group is a key feature, consisting of two phenyl rings attached to a phosphorus atom, which contributes to the compound's reactivity and stability. α-Lithium-trimethylsilylmethyldiphenylphosphin is used as a reagent in organic synthesis, particularly in the formation of carbon-phosphorus bonds and as a nucleophile in various chemical reactions. Due to its sensitivity, it requires careful handling and is often used in a controlled environment to prevent unwanted side reactions.

37820-40-9

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37820-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37820-40-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,8,2 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 37820-40:
(7*3)+(6*7)+(5*8)+(4*2)+(3*0)+(2*4)+(1*0)=119
119 % 10 = 9
So 37820-40-9 is a valid CAS Registry Number.

37820-40-9Downstream Products

37820-40-9Relevant academic research and scientific papers

Highly reactive scandium phosphinoalkylidene complex: C-H and H-H bonds activation

Mao, Weiqing,Xiang, Li,Lamsfus, Carlos Alvarez,Maron, Laurent,Leng, Xuebing,Chen, Yaofeng

, p. 1081 - 1084 (2017)

The first scandium phosphinoalkylidene complex was synthesized and structurally characterized. The complex has the shortest Sc-C bond lengths reported to date (2.089(3) ?). DFT calculations reveal the presence of a three center π interaction in the complex. This scandium phosphinoalkylidene complex undergoes intermolecular C-H bond activation of pyridine, 4-dimethylamino pyridine and 1,3-dimethylpyrazole at room temperature. Furthermore, the complex rapidly activates H2 under mild conditions. DFT calculations also demonstrate that the C-H activation of 1,3-dimethylpyrazole is selective for thermodynamic reasons and the relatively slow reaction is due to the need of fully breaking the chelating effect of the phosphino group to undergo the reaction whereas this is not the case for H2.

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