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2(3H)-Furanthione, dihydro-5-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

194725-10-5

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194725-10-5 Usage

Derivative of furan

Contains a furan ring with a sulfur atom and a hydrogen atom attached

Contains a phenyl group

A benzene ring with a substituent group attached

Used in production of pharmaceuticals and fragrances

Due to its chemical structure and properties, it can be used as a building block for creating various compounds

Potential applications in treatment of medical conditions

Has been studied for its potential use in treating neurological disorders and cancer

Investigated for antibacterial and antioxidant properties

Has been researched for its ability to inhibit bacterial growth and its potential to neutralize harmful free radicals

Important compound in medicinal chemistry

Due to its potential applications and versatility in creating various compounds, it is considered an important compound in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 194725-10-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,7,2 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 194725-10:
(8*1)+(7*9)+(6*4)+(5*7)+(4*2)+(3*5)+(2*1)+(1*0)=155
155 % 10 = 5
So 194725-10-5 is a valid CAS Registry Number.

194725-10-5SDS

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-phenyloxolane-2-thione

1.2 Other means of identification

Product number -
Other names 2(3H)-Furanthione,dihydro-5-phenyl

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:194725-10-5 SDS

194725-10-5Relevant academic research and scientific papers

Degradable vinyl copolymers through thiocarbonyl addition-ring-opening (TARO) polymerization

Bingham, Nathaniel M.,Roth, Peter J.

, p. 55 - 58 (2019)

The radical copolymerization of the thionolactone dibenzo[c,e]oxepane-5-thione with acrylates, acrylonitrile, and N,N-dimethylacrylamide afforded copolymers containing a controllable amount of backbone thioesters which could be selectively cleaved. The pr

Solvent-free thionation of γ-lactones under microwave irradiation

Filippi, Jean-Jacques,Fernandez, Xavier,Lizzani-Cuvelier, Louisette,Loiseau, André-Michel

, p. 6647 - 6650 (2003)

A series of γ-thionolactones was synthesized, with good yields, using a new combination of Lawesson's reagent (LR) and hexamethyldisiloxane (HMDO) in solvent-free conditions under microwave irradiation.

Reaction of thionolactones with zinc enolate: New synthesis of vinylogous carbonates

Lee, Hyeon Kyu,Kim, Jia,Pak, Chwang Siek

, p. 6267 - 6270 (2007/10/03)

Reaction of various thionolactones, prepared from the lactones and Lawesson's reagent, with methyl bromozinc-acetate afforded the corresponding vinylogous carbonates in good yields under mild conditions.

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