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2-Propenoic acid, 3-[(4-methylphenyl)sulfonyl]-, 2-propenyl ester, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106693-45-2

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106693-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106693-45-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,6,9 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 106693-45:
(8*1)+(7*0)+(6*6)+(5*6)+(4*9)+(3*3)+(2*4)+(1*5)=132
132 % 10 = 2
So 106693-45-2 is a valid CAS Registry Number.

106693-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (E) Allyl 3-p-toluenesulphonylacrylate

1.2 Other means of identification

Product number -
Other names (E)-3-(Toluene-4-sulfonyl)-acrylic acid allyl ester

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:106693-45-2 SDS

106693-45-2Relevant academic research and scientific papers

The effects of the carbonyl group in the cyclization of 1-hexenyl radicals

Serra,Da Silva Correa,Do Vale

, p. 9463 - 9488 (2007/10/02)

The radical chain cyclization of allyl ether derivatives promoted by tosyl halides and light is suppressed by the presence of one carbonyl group conjugated with the double bond (acrylic double bond).

1,3-DIPOLAR CYCLOADDITION REACTIONS OF PYRAZOLIDINIUM YLIDES WITH VINYL SULFONES. A REGIOSELECTIVE SYNTHESIS OF BICYCLIC PYRAZOLIDINONE ANTIBACTERIAL AGENTS

Jungheim, Louis N.,Barnett, Charles J.,Gray, Joseph E.,Horcher, Linus H.,Shepherd, Timothy A.,Sigmund, Sandra K.

, p. 3119 - 3126 (2007/10/02)

The 1,3-dipolar cycloaddition reaction of pyrazolidinium ylide 1 with substituted vinyl sulfones 5 was studied.Elimination of benzenesulfinic acid from the resulting cycloadducts gave rise to bicyclic pyrazolidinones 3.The (E)-olefin isomers were found to undergo cycloaddition in a highly regioselective fashion.These pyrazolidinones 3 represent the nuclei of an exciting new class of potent antibacterial agents that mimic β-lactams.

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