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3-Ethenyl-2,2-dimethyl-1-cyclopropanecarboxylic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60066-50-4

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60066-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60066-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,6 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 60066-50:
(7*6)+(6*0)+(5*0)+(4*6)+(3*6)+(2*5)+(1*0)=94
94 % 10 = 4
So 60066-50-4 is a valid CAS Registry Number.

60066-50-4SDS

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 ethyl 3-ethenyl-2,2-dimethylcyclopropane-1-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 3,3-dimethyl-2-vinylcyclopropanecarboxylate

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:60066-50-4 SDS

60066-50-4Downstream Products

60066-50-4Relevant academic research and scientific papers

Reactions of vinylcyclopropane epoxides with samarium and phosphorus iodides

Krief, Alain,Dumont, Willy,Baillieul, Diane

, p. 2688 - 2690 (2005)

Samarium diiodide on one hand, diphosphorus tetraiodide, and phosphorus triiodide on the other, react with vinylcyclopropane epoxides to produce either allylic alcohols or vinylcyclopropanes resulting from cyclopropane ring-opening or deoxygenation of the epoxide, respectively. Georg Thieme Verlag Stuttgart.

Process for preparing dihalovinylcyclopropanecarboxylates

-

, (2008/06/13)

Novel syntheses of dihalovinylcyclopropanecarboxylates, including potent insecticides, are described. The processes begin with the reaction between an alkenol and an orthoester to produce a γ-unsaturated carboxylate, followed by the catalyzed addition of a carbon tetrahalide to the double bond and dehydrohalogenation to produce a cyclopropane derivative.

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