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Ethanone, 1-spiro[1,3-benzoxathiole-2,1'-cyclopentan]-5-yl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91870-97-2

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91870-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91870-97-2 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 91870-97:
(7*9)+(6*1)+(5*8)+(4*7)+(3*0)+(2*9)+(1*7)=162
162 % 10 = 2
So 91870-97-2 is a valid CAS Registry Number.

91870-97-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-acetylspiro(1,3-benzoxathiole-2,1'-cyclopentane)

1.2 Other means of identification

Product number -
Other names 5-acetylspiro(1,3-benzoxathiole-2,1'-cyclopentane)

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:91870-97-2 SDS

91870-97-2Downstream Products

91870-97-2Relevant articles and documents

Studies on the Synthesis of Heterocyclic Compounds. XVI. Cleavage of 1,3-Benzodioxoles and -Benzoxathioles by Sodium Iodide-Acyl Chloride

Corda, Luciana,Fadda, Anna Maria,Maccioni, Antonio,Maccioni, Anna Maria,Podda, Gianni

, p. 311 - 314 (2007/10/02)

The cleavage reaction of ethereal and thioethereal bonds with sodium iodide and acyl chloride has been studied.In all the 1,3-benzodioxoles and -benzoxathioles studied, the opening of the heterocyclic ring with formation of 1,2-diacetoxybenzene or 2-hydroxythiophenol diacetic acid ester and gem-diiodoalkanes and iodoalkenes has been observed.The structure of newly prepared compounds has been determined by analytical and spectroscopic data or comparison with authentic samples.

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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