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Ethanone, 1-(2-methyl-1,3-oxathiolan-2-yl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33266-06-7

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33266-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33266-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,2,6 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 33266-06:
(7*3)+(6*3)+(5*2)+(4*6)+(3*6)+(2*0)+(1*6)=97
97 % 10 = 7
So 33266-06-7 is a valid CAS Registry Number.

33266-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-acetyl-2-methyl-1,3-oxathiolane

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:33266-06-7 SDS

33266-06-7Downstream Products

33266-06-7Relevant academic research and scientific papers

Preparation of Some Oxa- and Thia-decalins and -propellanes. Barriers to Conformational Interconversion

Fjeldskaar, Inger Reidun,Skatteboel, Lars

, p. 410 - 417 (2007/10/02)

Reactions of 5,6-dihydro-2,3-dimethyl-1,4-dioxin, -1,4-oxathiin and -1,4-dithiin with bromine in the presence of 1,2-ethanediol, 2-mercaptoethanol and 1,2-ethanedithiol, respectively, afforded, in most cases, high yields of the corresponding oxa- and thia-decalins as cis-isomers only.Similar reactions of the bicyclic dihydrodioxins, 2,5-dioxabicyclodec-1(6)-ene and the sulfur analogues gave the corresponding propellanes in high yields.The barriers to conformational interconversion were obtained from variable temperature NMR spectra.Other examples of propellanes were obtained; addition of dihalocarbenes to the bicyclic dihydrodioxins furnished the corresponding dihalocyclopropane derivatives, and the photochemical addition of benzophenone gave the expected oxetane.

Electron Impact Induced Fragmentations of Some 2,2-disubstituted 1,3-oxathiolanes

Vainiotalo, Pirjo,Nevalainen, Vesa

, p. 467 - 472 (2007/10/02)

The electron impact induced fragmentations of nine 2,2-disubstituted 1,3-oxathiolanes have been studied by means of exact mass measurement and metastable ion analysis.The ring cleavage almost always takes place so that the C(2)-S and C(5)-O bonds are brok

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