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dimethyl(tert-butyl)aminosilane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18182-35-9

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18182-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18182-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,8 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18182-35:
(7*1)+(6*8)+(5*1)+(4*8)+(3*2)+(2*3)+(1*5)=109
109 % 10 = 9
So 18182-35-9 is a valid CAS Registry Number.

18182-35-9Relevant academic research and scientific papers

Expanding the Library of Uranyl Amide Derivatives: New Complexes Featuring the tert -Butyldimethylsilylamide Ligand

Pattenaude, Scott A.,Coughlin, Ezra J.,Collins, Tyler S.,Zeller, Matthias,Bart, Suzanne C.

, p. 4543 - 4549 (2018)

New uranyl derivatives featuring the amide ligand, -N(SiHMe2)tBu, were synthesized and characterized by X-ray crystallography, multinuclear NMR spectroscopy, and absorption spectroscopies. Steric properties of these complexes were also quantified using the computational program Solid-G. The increased basicity of the free ligand -N(SiHMe2)tBu was demonstrated by direct comparison to -N(SiMe3)2, a popular supporting ligand for uranyl. Substitutional lability on a uranyl center was also demonstrated by exchange with the -N(SiMe3)2 ligand. The increased basicity of this ligand and diverse characterization handles discussed here will make these compounds useful synthons for future reactivity.

Ion-molecule reactions of monosubstituted ethylsilylium ions with trimethyl(tert-butylamino)silane in the gas phase

Kochina,Shchukin,Nefedov,Sinotova

, p. 1233 - 1236 (2007/10/03)

Reaction of nuclear-chemically generated ethylsilylium ions with trimethyl(rert-butylamino)silane in the gas phase was studied. In the course of reaction the ethylsilylium ion completely isomerizes into the dimethylsilylium ion. Experiments show that the pathway involving proton transfer practically is not realized, in contrast to the reactions of carbenium ions with amines.

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