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Cyclopentanone, 3-(dimethylphenylsilyl)-3-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67263-03-0

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67263-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67263-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,6 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 67263-03:
(7*6)+(6*7)+(5*2)+(4*6)+(3*3)+(2*0)+(1*3)=130
130 % 10 = 0
So 67263-03-0 is a valid CAS Registry Number.

67263-03-0SDS

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 3-(dimethyl(phenyl)silyl)-3-methylcyclopentanone

1.2 Other means of identification

Product number -
Other names 3-dimethyl(phenyl)silyl-3-methylcyclopentanone

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:67263-03-0 SDS

67263-03-0Relevant academic research and scientific papers

Conjugate additions of a simple monosilylcopper reagent with use of the CuI-DMS complex: Stereoselectivities and a dramatic impact by DMS

Dambacher, Jesse,Bergdahl, Mikael

, p. 580 - 589 (2007/10/03)

(Chemical Equation Presented) Conjugate additions utilizing the simple monosilylcuprate reagent Li[PhMe2SiCuI] to α,β-unsaturated carbonyl compounds are described. The presence of dimethyl sulfide (DMS), either as a component originating from t

The Conjugate Addition of a Silyl Group to Enones and its Removal with Copper(II) Bromide: A Protecting Group for the αβ-Unsaturation of αβ-Unsaturated Ketones

Ager, David J.,Fleming, Ian,Patel, Shailesh K.

, p. 2520 - 2526 (2007/10/02)

Silyl-lithium reagents mixed with copper(I) salts react with enones, including esters and aldehydes, to give β-silyl carbonyl compounds in good yield.The β-silylketones can be used in synthesis without risk to the silyl group and the enone group can be restored by bromination-desilylbromination with copper(II) bromide.The principle is illustrated with syntheses of carvone and dihydrojasmone.

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