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4-(4,4-diphenyl-4-silacyclohexyl)cyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

174458-50-5

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174458-50-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 174458-50-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,4,5 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 174458-50:
(8*1)+(7*7)+(6*4)+(5*4)+(4*5)+(3*8)+(2*5)+(1*0)=155
155 % 10 = 5
So 174458-50-5 is a valid CAS Registry Number.

174458-50-5Upstream product

174458-50-5Relevant academic research and scientific papers

Cyclohexanone compounds, process for preparing the same, and processes for preparing silacyclohexane-based liquid crystal compounds from the cyclohexanone compounds

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, (2008/06/13)

A cyclohexanone compound of the following general formula (I) is provided STR1 wherein Ar represents a phenyl group or a tolyl group, and R represents a phenyl group, a tolyl group, a linear alkyl group having from 1 to 10 carbon atoms, a mono or difluoroalkyl group having from 1 to 10 carbon atoms, a branched alkyl group having from 3 to 8 carbon atoms or an alkoxyalkyl group having from 2 to 7 carbon atoms. The preparation of the cyclohexanone compound is also described along with processes for preparing liquid crystal compounds from the cyclohexanone compound.

Process for preparing sil acyclohexane-based liquid crystal compounds from silacyclohexanone compounds

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, (2008/06/13)

Silacyclohexane-based liquid crystal compounds are prepared from a cyclohexanone compound of the following general formula (I) wherein Ar represents a phenyl group or a tolyl group, and R represents a phenyl group, a tolyl group, a linear alkyl group having from 1 to 10 carbon atoms, a mono or difluoroalkyl group having from 1 to 10 carbon atoms, a branched alkyl group having from 3 to 8 carbon atoms or an alkoxyalkyl group having from 2 to 7 carbon atoms, and also from organolithium reagents, followed by hydrogenolysis or hydrogenation after dehydration, with or without further reaction with organometal reagents, and then to de-silylation and reduction.

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