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Pyridine, 2-[(1,1-dimethylethyl)dimethylsilyl]- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

134435-17-9

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134435-17-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134435-17-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,4,3 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 134435-17:
(8*1)+(7*3)+(6*4)+(5*4)+(4*3)+(3*5)+(2*1)+(1*7)=109
109 % 10 = 9
So 134435-17-9 is a valid CAS Registry Number.

134435-17-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(tert-butyldimethylsilyl)pyridine

1.2 Other means of identification

Product number -
Other names 2-t-butyldimethylsilylpyridine

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:134435-17-9 SDS

134435-17-9Relevant academic research and scientific papers

Preparation of Tricarbonyl(η6-pyridine)chromium(0) Complexes

Davies, Stephen G.,Shipton, Mark R.

, p. 501 - 507 (1991)

The synthesis of tricarbonyl(η6-pyridine)chromium(0) complexes is accomplished via complexation of 2-silylpyridines with subsequent fluoride ion-mediated desilylation under mild conditions.The tricarbonylchromium(0) complexes of pyridine, 2-methylpyridine, 3-methylpyridine, 2-ethylpyridine, 2-(but-3-enyl)pyridine and 2-(6-trimethylsilylpyridyl)-1,3-dioxolane are prepared.Deprotonation (lithium diisopropylamide) and methylation (methyl iodide) of tricarbonyl(η6-pyridine)chromium(0) converts it cleanly to tricarbonyl(η6-2-methylpyridine)chromium(0).

Photochemical C-H Silylation and Hydroxymethylation of Pyridines and Related Structures: Synthetic Scope and Mechanisms

Rammal, Fatima,Gao, Di,Boujnah, Sondes,Hussein, Aqeel A.,Lalevée, Jacques,Gaumont, Annie-Claude,Morlet-Savary, Fabrice,Lakhdar, Sami

, p. 13710 - 13717 (2020/11/30)

Considering the synthetic relevance of heteroarenes in various areas ranging from organic synthesis to medicinal chemistry, developing practically simple methodologies to access functionalized heteroarenes is of a significant value. Described herein is an efficient approach for C-H silylation and hydroxymethylation of pyridines and related heterocycles by the combination of silanes or methanol with readily available N-methoxypyridinium ions with a low catalyst loading (2 mol %) under blue light irradiation. The synthetic importance of the developed reactions is demonstrated by the synthesis of biologically relevant compounds. Electron paramagnetic resonance spectroscopy, quantum yield measurements, and density-functional theory calculations allowed us to understand reaction mechanisms of both photocatalytic reactions.

Palladium-mediated olefination of 2-(tert-butyldimethylsilyl)pyridine by sp3 C-H activation

Wang, Cong,Ge, Haibo

experimental part, p. 2590 - 2594 (2011/10/02)

An unprecedented direct alkenylation of 2-(tert-butyl-dimethylsilyl) pyridine with acrylates through palladium-mediated C-H activation on a nonacidic sp3 carbon is reported. This method provides an efficient approach to allylsilanes. Georg Thie

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