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Z-3-(triphenylsilyl)indenethione S-oxide is a complex organic compound characterized by its unique molecular structure. It features a tricyclic core with a sulfur atom incorporated into the molecule, which is essential for its chemical properties. The compound is notable for its S-oxide functionality, indicating that one of the sulfur atoms is bonded to an oxygen atom, which can influence its reactivity and stability. The presence of a triphenylsilyl group, which consists of three phenyl rings attached to a silicon atom, further enhances the compound's steric and electronic properties. This group can provide stability and can also act as a protecting group in organic synthesis, making it a potentially valuable intermediate in the synthesis of more complex molecules. The compound's structure and properties make it an interesting subject for study in the field of organic chemistry, particularly in the context of sulfur-containing compounds and their applications.

89523-81-9

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89523-81-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89523-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,2 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89523-81:
(7*8)+(6*9)+(5*5)+(4*2)+(3*3)+(2*8)+(1*1)=169
169 % 10 = 9
So 89523-81-9 is a valid CAS Registry Number.

89523-81-9Downstream Products

89523-81-9Relevant academic research and scientific papers

Synthesis of α,β-unsaturated sulfines from silylindenes and sulfur dioxide

Porskamp, P. A. T. W.,Wijdeven, A. M. van de,Zwanenburg, B.

, p. 506 - 510 (2007/10/02)

The synthesis of a variety of substituted indenethione S-oxide (all α,β-unsaturated sulfines) is described.Essentially these sulfines are prepared by the reaction of α-silyl carbanions with an excess of sulfur dioxide (modified Peterson reaction).The requisite α-silyl carbanions are generated by two different routes, i.e. by α-deprotonation of trimethylsilyl-substituted indenes and by nucleophilic δ-addition of alkyllithium compounds to dienesilanes.In all cases, the sulfines prepared were converted into cycloadducts by reaction with 2,3-dimethyl-1,3-butadiene.

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