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α-Triethylsilyl-N-phenylacetamide is an organic compound with the molecular formula C14H23NOSi. It is a derivative of N-phenylacetamide, featuring a triethylsilyl group (Si(C2H5)3) attached to the α-carbon atom. This modification introduces unique chemical properties, such as increased lipophilicity and steric hindrance, which can affect its reactivity and interactions with other molecules. The compound is synthesized by reacting N-phenylacetamide with triethylsilyl chloride in the presence of a base, and it is used in various chemical reactions and as a protecting group in organic synthesis. Its structure and properties make it a valuable tool in the development of new pharmaceuticals and other chemical compounds.

24082-13-1

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24082-13-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24082-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,8 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24082-13:
(7*2)+(6*4)+(5*0)+(4*8)+(3*2)+(2*1)+(1*3)=81
81 % 10 = 1
So 24082-13-1 is a valid CAS Registry Number.

24082-13-1Downstream Products

24082-13-1Relevant academic research and scientific papers

Lewis Acid-Activated Reactions of Silyl Ketenes for the Preparation of α-Silyl Carbonyl Compounds

Mitchell, Sarah M.,Xiang, Yuanhui,Matthews, Rachael,Amburgey, Alexis M.,Pentzer, Emily B.

, (2019/11/14)

Silyl-substituted ketenes are attractive molecular building blocks due to their stability and ease of storage, as opposed to unstable alkyl and aryl ketenes. To better understand the reactivity of silyl ketenes and, in turn, their use in the preparation o

Lewis Acid-Activated Reactions of Silyl Ketenes for the Preparation of α-Silyl Carbonyl Compounds

Mitchell, Sarah M.,Xiang, Yuanhui,Matthews, Rachael,Amburgey, Alexis M.,Pentzer, Emily B.

, p. 14461 - 14468 (2019/12/02)

Silyl-substituted ketenes are attractive molecular building blocks due to their stability and ease of storage, as opposed to unstable alkyl and aryl ketenes. To better understand the reactivity of silyl ketenes and, in turn, their use in the preparation o

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