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Cyclohexanol, 1-[2-(trimethylsilyl)ethenyl]-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87428-68-0

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87428-68-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87428-68-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,2 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87428-68:
(7*8)+(6*7)+(5*4)+(4*2)+(3*8)+(2*6)+(1*8)=170
170 % 10 = 0
So 87428-68-0 is a valid CAS Registry Number.

87428-68-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-trimethylsilylethyen-1-yl)-1-hydroxycyclohexane

1.2 Other means of identification

Product number -
Other names trans-1-(2-trimethylsilyl)vinyl-1-cyclohexanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:87428-68-0 SDS

87428-68-0Relevant academic research and scientific papers

1-LITHIO-1-BENZENESULFINYL-2-TRIMETHYLSILYLETHANE AS A 2-TRIMETHYLSILYLVINYL ANION EQUIVALENT IN REACTIONS WITH ALHEDYDES, KETONES AND EPOXIDES

Hsiao, C-N.,Shechter, H.

, p. 2371 - 2374 (2007/10/02)

Aldehydes, ketones and epoxides give adducts with 1-lithio-1-benzenesulfinyl-2-trimethylsilylethane which upon neutralization eliminate benezenesulfenic acid efficiently at 76 deg C to yield trans-3-(trimethylsilyl)allyl alcohols and trans-4-(trimethylsilyl)-3-alken-1-ols.

A NEW SYNTHESIS OF UNSATURATED ALDEHYDES

Cutting, Ian,Parsons, Philip J.

, p. 2021 - 2022 (2007/10/02)

Treatment of 3-trimethylsilylallylic alcohols with phenylsulphenyl chloride gives unstable allylic sulphoxides which rearrange and are then hydrolysed to unsaturated aldehydes.

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