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Silane, [[4-(3,5-dimethylphenyl)-1-butynyl]oxy]tris(1-methylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

765906-53-4

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765906-53-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 765906-53-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,5,9,0 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 765906-53:
(8*7)+(7*6)+(6*5)+(5*9)+(4*0)+(3*6)+(2*5)+(1*3)=204
204 % 10 = 4
So 765906-53-4 is a valid CAS Registry Number.

765906-53-4SDS

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 4-(3,5-dimethylphenyl)but-1-ynoxy-tri(propan-2-yl)silane

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:765906-53-4 SDS

765906-53-4Downstream Products

765906-53-4Relevant academic research and scientific papers

Bronsted acid-promoted cyclizations of siloxyalkynes with arenes and alkenes

Zhang, Liming,Kozmin, Sergey A.

, p. 10204 - 10205 (2007/10/03)

We have described the first Bronsted acid-mediated cyclizations of siloxyalkynes with simple arenes and alkenes to afford substituted tetralone and cyclohexenone derivatives. The most notable aspect of the carbocyclizations involving siloxyalkynes is the ability to employ a range of substrates that are not restricted to those containing electron-rich arenes and alkenes. The key mechanistic feature of the reaction is the generation of a highly reactive ketenium ion upon protonation of siloxyalkyne. We believe that the low nucleophilicty of the counteranion is crucial for enabling the formation and effective interception of this highly reactive intermediate. Copyright

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