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Silane, trimethyl(1-oxo-3-phenyl-2-propenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66132-97-6

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66132-97-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66132-97-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,1,3 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66132-97:
(7*6)+(6*6)+(5*1)+(4*3)+(3*2)+(2*9)+(1*7)=126
126 % 10 = 6
So 66132-97-6 is a valid CAS Registry Number.

66132-97-6Relevant academic research and scientific papers

Stereoselective synthesis of allyl ethers using α,β-unsaturated acylsilanes

Honda, Mitsunori,Takatera, Takehide,Ui, Ryosuke,Kunimoto, Ko-Ki,Segi, Masahito

, p. 864 - 869 (2017/02/18)

The reaction behavior of silylvinylmethanols with acid catalysts was investigated. The starting silylvinylmethanols 2 were prepared by the reaction of the corresponding α,β-unsaturated acylsilanes 1 with organocerium reagents. The reaction of 2 with TsOH

Synthesis and reactivity of iron carbonyl complexes of α,β-unsaturated acyl silanes

Thomas, Susan E.,Tustin, Gary J.,Ibbotson, Arthur

, p. 7629 - 7640 (2007/10/02)

2-Trimethylsilyl-1-oxa-1,3-butadiene (7) reacts with Fe2(CO)9 to form an unstable tetracarbonyliron (0) complex (8) whereas 2-trimethylsilyl-4-phenyl-1-oxa- 1-oxa-1,3-butadiene (9) and 2-(tert-butyldimethylsilyl)-4-phenyl-1-oxa-1,3-butadiene (20) react with Fe2(CO)9 to form highly stable crystalline tricarbonyliron(0) complexes (16 and (21). Complexes (16) and (21) both undergo acylation when reacted with methyl lithium under nitrogen to form γ-ketoacylsilanes [(18) and (22)], but only complex (21) reacts with methyl lithium under carbon monoxide to give the tricarbonyl(vinylketene)iron(0) complex (23).

Rearrangement of allylic and propargylic alcohols catalyzed by the combined use of tetrabutylammonium perrhenate(VII) and p-toluenesulfonic acid

Narasaka,Kusama,Hayashi

, p. 2059 - 2068 (2007/10/02)

Allylic rearrangement and/or dehydration reaction of allylic alcohols proceeds smoothly by the use of catalytic amounts of tetrabutylammonium perrhenate and p-toluenesulfonic acid hydrate. Treatment of propargylic alcohols with the catalysts at room temperature affords the rearranged products, α,β-unsaturated carbonyl compounds, while β,γ-unsaturated ketones are obtained as main products by the reaction in refluxing 1,2-dichloroethane. The application of this catalytic system is also described for the preparation of some synthetic intermediates.

Rearrangement of Allylic and Propargylic Alcohols Catalyzed by the Combined Use of Tetrabutylammonium Perrhenate(VII) and p-Toluenesulfonic Acid

Narasaka, Koichi,Kusama, Hiroyuki,Hayashi, Yujiro

, p. 1413 - 1416 (2007/10/02)

Allylic rearrangement and/or dehydration of allylic alcohols proceed by the use of a catalytic amount of tetrabutylammonium perrhenate and p-toluenesulfonic acid.Treatment of propargylic alcohols with the above reagents affords the rearranged products, α,β-unsaturated carbonyl compounds.

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