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Z-3-(1,1-diphenylethyl)indenethione S-oxide is a complex organic chemical compound with the molecular formula C25H21OS. It is characterized by a unique structure that includes an indenethione core, which is a sulfur-containing derivative of indene, and a 1,1-diphenylethyl group attached to the 3-position of the indene ring. Z-3-(1,1-diphenylethyl)indenethione S-oxide is of interest in the field of organic chemistry, particularly for its potential applications in the synthesis of pharmaceuticals and other specialty chemicals. Its S-oxide form indicates the presence of a sulfur atom in an oxidized state, which can influence its reactivity and properties. The compound's specific applications and properties are not widely documented, suggesting it may be a research chemical or an intermediate in the synthesis of more complex molecules.

89524-01-6

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89524-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89524-01-6 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 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89524-01:
(7*8)+(6*9)+(5*5)+(4*2)+(3*4)+(2*0)+(1*1)=156
156 % 10 = 6
So 89524-01-6 is a valid CAS Registry Number.

89524-01-6Downstream Products

89524-01-6Relevant 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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