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1-Propanone, 1-phenyl-3-(phenylthio)-3-(trimethylsilyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86029-78-9

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86029-78-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86029-78-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,0,2 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86029-78:
(7*8)+(6*6)+(5*0)+(4*2)+(3*9)+(2*7)+(1*8)=149
149 % 10 = 9
So 86029-78-9 is a valid CAS Registry Number.

86029-78-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name β-phenylthio-β-trimethylsilylpropiophenone

1.2 Other means of identification

Product number -
Other names -

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:86029-78-9 SDS

86029-78-9Relevant academic research and scientific papers

Chloro(phenylthio)methyltrimethylsilane: Preparation and some Synthetic Reactions

Yamamoto, Iwao,Okuda, Kazuhide,Nagai, Shigemasa,Motoyoshiya, Jiro,Gotoh, Haruo,Matsuzaki, Kei

, p. 435 - 438 (2007/10/02)

Reaction of the title compound (2) with lead thiocyanate gave phenylthio(trimethylsilyl)methyl isothiocyanate (3) which further reacted with aromatic aldehydes in the presence of fluoride ion to afford oxazoles in good yields.Compound (2) also reacted with silyl enol ethers to give β-silyl ketones which were capable of being converted into β-functionalized vinylsilanes.

THE PREPARATION β-KETOALDEHYDES

Ager, David J.

, p. 419 - 422 (2007/10/02)

β-Ketoaldehydes(7) were prepared by the addition of bromophenylthiotrimethylsilylmethane(6) to trimethylsilyl enol ethers(3) followed by a sila-Pummerer rearrangement and hydrolysis.

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