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

105598-46-7

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105598-46-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105598-46-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,5,9 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 105598-46:
(8*1)+(7*0)+(6*5)+(5*5)+(4*9)+(3*8)+(2*4)+(1*6)=137
137 % 10 = 7
So 105598-46-7 is a valid CAS Registry Number.

105598-46-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(allyloxy)-3-methylcyclohexene

1.2 Other means of identification

Product number -
Other names 3-Allyloxy-3-methyl-cyclohexene

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:105598-46-7 SDS

105598-46-7Downstream Products

105598-46-7Relevant academic research and scientific papers

Synthesis of Cyclobutanated Butyrolactones via Copper(I)-Catalyzed Intermolecular Photocycloadditions of Homoallyl Vinyl or Diallyl Ethers

Ghosh, Subrata,Raychaudhuri, Swadesh R.,Salomon, Robert G.

, p. 83 - 90 (2007/10/02)

Intramolecular copper(I)-catalyzed 2? + 2? photocycloaddition provides an effective route for the synthesis of 2-oxa- and 3-oxabicycloheptanes from homoallyl vinyl or diallyl ethers, respectively.Ruthenium-catalyzed oxidation of these multicyclic tetrahydrofuran products provides a novel annulation of cyclobutanated butyrolactones.For intermediates incorporating both methine and methylene groups next to the tetrahydrofuran oxygen, a remarkable selectivity was found for oxidation at the methylene position.Highly stereoselective generation of exo-2-alkylsubstituted 3-oxabicycloheptanes occurred upon photobicyclization of diallyl ethers bearing an α-alkyl substituent.

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