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200192-51-4

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200192-51-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 200192-51-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,1,9 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 200192-51:
(8*2)+(7*0)+(6*0)+(5*1)+(4*9)+(3*2)+(2*5)+(1*1)=74
74 % 10 = 4
So 200192-51-4 is a valid CAS Registry Number.

200192-51-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl-(1-phenylbut-3-enoxy)-prop-2-enylsilane

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:200192-51-4 SDS

200192-51-4Relevant articles and documents

Homoallyl-cyclopropylcarbinyl cation manifold. Trimethylsilyl versus aryl stabilization

Creary, Xavier,O'Donnell, Benjamin D.,Vervaeke, Marie

, p. 3360 - 3368 (2008/02/03)

(Chemical Equation Presented) A series of E- and Z-1-aryl-5-trimethylsilyl- 3-buten-1-yl trifluoroacetates were solvolyzed in CD3CO2D, and rates of reaction as well as products derived from these reactions were determined. Hammett pl

Stereoselective synthesis of 2,3,5-trisubstituted tetrahydrofurans by an allyl silane metathesis - Nucleophilic addition sequence

Cassidy, John H.,Marsden, Stephen P.,Stemp, Geoffrey

, p. 1411 - 1413 (2007/10/03)

Functionalised cyclic allyl silanes have been prepared by the ring closing metathesis of allyldimethylsilyl ethers of homoallylic alcohols. Treatment of these allyl silanes with aldehydes in the presence of boron trifluoride etherate gives high yields of

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