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2,2-Dimethyl-1,3-oxathiolan-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35350-46-0

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35350-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35350-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,5 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35350-46:
(7*3)+(6*5)+(5*3)+(4*5)+(3*0)+(2*4)+(1*6)=100
100 % 10 = 0
So 35350-46-0 is a valid CAS Registry Number.

35350-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethyl-[1,3]oxathiolan-5-one

1.2 Other means of identification

Product number -
Other names 2,2-Dimethyl-5-oxo-1,3-oxathiolan

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:35350-46-0 SDS

35350-46-0Relevant academic research and scientific papers

COMPOUNDS FOR USE IN THE TREATMENT OF INFECTIOUS DISEASES

-

Page/Page column 77-78, (2016/05/02)

The present invention relates to compounds of formula (I), wherein R1, R2, R3, R4, R5 and R6 are as described herein, and their prodrugs or pharmaceutically acceptable salt, enantiomer or diastereomer thereof, and compositions including the compounds and methods of using the compounds.

2-Mercaptoaldehyde dimers and 2,5-dihydrothiophenes from 1,3-oxathiolan-5-ones

McIntosh, John M.,Siddiqui, Maqbool A.

, p. 1872 - 1875 (2007/10/02)

Representative 1,3-oxathiolan-5-ones (6), prepared from 2-mercaptoacids, have been reduced to 2-mercaptoaldehydes 1 with diisobutylaluminum hydride.The aldehydes 1, which appear to exist in several dimeric forms, react with vinyltriphenylphosphonium bromide to give 2,5-dihydrothiophenes.

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