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3-Undecanone, 2-(trimethylsilyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86997-45-7

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86997-45-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86997-45-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,9 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 86997-45:
(7*8)+(6*6)+(5*9)+(4*9)+(3*7)+(2*4)+(1*5)=207
207 % 10 = 7
So 86997-45-7 is a valid CAS Registry Number.

86997-45-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-trimethylsilylundecan-3-one

1.2 Other means of identification

Product number -
Other names 3-Undecanone,2-(trimethylsilyl)

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:86997-45-7 SDS

86997-45-7Downstream Products

86997-45-7Relevant academic research and scientific papers

Reaction of acylsilanes with sulfur ylides. Selective formation of silyl enol ethers or β-ketosilanes

Nakajima, Tadashi,Segi, Masahito,Sugimoto, Fumitosi,Hioki, Reiko,Yokota, Seiko,Miyashita, Kiyoshi

, p. 8343 - 8358 (2007/10/02)

The reaction of acylsilanes with sulfur ylides in THF results in the formation of the corresponding silyl enol ethers or β-ketosilanes. The relative ratio of these products varies with the ylide conditions and the stability of ylide used. It is noteworthy that silyl enol ethers were formed under the salt-free ylide conditions, and that β-ketosilanes were yielded in the presence of soluble inorganic salts in THF, selectively. The formation of both products would be interpreted in terms of the anionotropic and cationotropic rearrangements of silyl group in the reaction intermediate.

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