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Triphenylsilyl ketene is an organosilicon compound with the chemical formula (C6H5)3SiCO. It is a derivative of ketene, featuring a silicon atom bonded to three phenyl groups and a carbonyl group. triphenylsilyl ketene is known for its stability and reactivity, which makes it a valuable intermediate in organic synthesis. It can be used in the preparation of various organic compounds, particularly those containing a silicon-carbon bond. Triphenylsilyl ketene is also notable for its ability to participate in reactions such as [2+2] cycloadditions and insertion reactions, making it a versatile building block in the synthesis of complex molecules.

42414-76-6

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42414-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42414-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,4,1 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42414-76:
(7*4)+(6*2)+(5*4)+(4*1)+(3*4)+(2*7)+(1*6)=96
96 % 10 = 6
So 42414-76-6 is a valid CAS Registry Number.

42414-76-6Downstream Products

42414-76-6Relevant 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.

, p. 14461 - 14468 (2019)

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.

, (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

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