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18391-77-0

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18391-77-0 Usage

General Description

1-methyl-3-phenyl-2-thioxoimidazolidin-4-one, also known as tioxolone, is a chemical compound with the molecular formula C10H11NO2S. It is a derivative of imidazolidine-2-thione and is commonly used in the pharmaceutical industry for its potential as an anti-inflammatory, antiviral, and antifungal agent. Tioxolone has also been studied for its potential as a treatment for acne, psoriasis, and other skin conditions. Its unique structure and properties make it a promising candidate for the development of new drugs and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 18391-77-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,9 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18391-77:
(7*1)+(6*8)+(5*3)+(4*9)+(3*1)+(2*7)+(1*7)=130
130 % 10 = 0
So 18391-77-0 is a valid CAS Registry Number.

18391-77-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-3-phenyl-2-sulfanylideneimidazolidin-4-one

1.2 Other means of identification

Product number -
Other names 1-Methyl-3-phenyl-2-thioxo-imidazolidin-4-on

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:18391-77-0 SDS

18391-77-0Relevant articles and documents

Synthesis and biological evaluation of 3-substituted 5-benzylidene-1-methyl-2-thiohydantoins as potent NADPH oxidase (NOX) inhibitors

Bae, Yun Soo,Choi, Sun,Park, Jung Jae,Joo, Jung Hee,Cui, Minghua,Cho, Hyunsung,Lee, Won Jae,Lee, Sang Hyup

, p. 4144 - 4151 (2016/08/23)

We report the synthesis of novel 3-substituted 5-benzylidene-1-methyl-2-thiohydantoins 3, and their biological evaluation using NADPH oxidase (NOX) 1 and 4. Based on structural and pharmacophore analyses of known inhibitors such as hydroxypyrazole 2, we e

Synthesis of 3-substituted 5-arylidene-1-methyl-2-Thiohydantoins under microwave irradiation

Khodair, Ahmed I.,Nielsen, John

, p. 1017 - 1032 (2007/10/03)

A mono-modal microwave oven was used to expedite the synthesis of small libraries of 3-substituted 1-methyl-2-thiohydantoins and 3-substituted 5-arylidene-1-methyl-2-thiohydantoins. In comparison with the traditional reflux methods, similar or higher yields were obtained.

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