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91870-93-8

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91870-93-8 Usage

General Description

Ethanone, 1-(2-ethyl-2-methyl-1,3-benzoxathiol-5-yl)- is a unique chemical compound that contains a benzoxathiol ring with an ethyl and methyl group attached. Ethanone, 1-(2-ethyl-2-methyl-1,3-benzoxathiol-5-yl)- is a ketone with a sulfur-containing heterocycle, giving it potentially interesting properties for pharmaceutical or industrial applications. The structure of this compound suggests that it may have both aromatic and aliphatic properties, making it potentially useful in a variety of chemical reactions. Further research into the specific properties and potential uses of this compound could uncover its full potential in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 91870-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,8,7 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91870-93:
(7*9)+(6*1)+(5*8)+(4*7)+(3*0)+(2*9)+(1*3)=158
158 % 10 = 8
So 91870-93-8 is a valid CAS Registry Number.

91870-93-8SDS

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 1-(2-ethyl-2-methylbenzo[d][1,3]oxathiol-5-yl)ethan-1-one

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

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More Details:91870-93-8 SDS

91870-93-8Downstream Products

91870-93-8Relevant articles and documents

On the Acylation of 1,3-Benzoxathiole Systems

Bernard, Angela Maria,Cocco, Maria Teresa,Congiu, Cenzo,Plumitallo, Antonio

, p. 591 - 593 (2007/10/02)

The acylation on 1,3-benzoxathiole systems, as well as the effect of the stoichiometry of the catalyst on the yields of ketones and of breaking products of the O-C-S bonds is here described.

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