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2(3H)-Furanone, dihydro-3-[(methylsulfonyl)oxy]-, (3R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

192057-37-7

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192057-37-7 Usage

Molecular Structure

Furanone ring and methylsulfonyl group

Odor

Fruity and sweet

Usage

Flavoring agent in food and beverages, production of perfumes and fragrance products

Properties

Antibacterial and antifungal

Potential Applications

Pharmaceuticals and personal care products

Check Digit Verification of cas no

The CAS Registry Mumber 192057-37-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,0,5 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 192057-37:
(8*1)+(7*9)+(6*2)+(5*0)+(4*5)+(3*7)+(2*3)+(1*7)=137
137 % 10 = 7
So 192057-37-7 is a valid CAS Registry Number.

192057-37-7SDS

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 [(3R)-2-oxooxolan-3-yl] methanesulfonate

1.2 Other means of identification

Product number -
Other names methanesulfonic acid (3R)-2-oxotetrahydrofuran-3-yl 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:192057-37-7 SDS

192057-37-7Relevant academic research and scientific papers

Novel glucocorticoid antedrugs possessing a 21-(γ-lactone) ring

Angell, Richard M.,Biggadike, Keith,Farrell, Rosanne M.,Flack, Stephen S.,Hancock, Ashley P.,Irving, Wendy R.,Lynn, Sean M.,Procopiou, Panayiotis A.

, p. 831 - 839 (2007/10/03)

Pregnane derivatives bearing γ-butyrolactones at C21 were prepared and tested as glucocorticoid agonists. The compounds were also tested for their liability in human plasmas. The compounds were found to be rapidly hydrolyzed by the enzyme paraoxonase to the respective hydroxyacids.

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