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[(2-phenylquinolin-4-yl)sulfanyl]acetic acid is a chemical compound characterized by the molecular formula C18H13NO2S. It is a derivative of sulfanylacetic acid, featuring a quinoline ring with a phenyl group attached at the 2-position. [(2-phenylquinolin-4-yl)sulfanyl]acetic acid holds promise in the realm of medicinal chemistry and drug development due to its demonstrated antioxidant and anti-inflammatory properties.

5443-03-8

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5443-03-8 Usage

Uses

Used in Pharmaceutical Synthesis:
[(2-phenylquinolin-4-yl)sulfanyl]acetic acid is utilized as a key intermediate in the synthesis of various pharmaceuticals and bioactive compounds. Its unique structure and properties make it a valuable building block for creating novel drugs with potential therapeutic applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [(2-phenylquinolin-4-yl)sulfanyl]acetic acid is employed as a compound with antioxidant and anti-inflammatory properties. These characteristics are crucial for the development of drugs targeting conditions associated with oxidative stress and inflammation, such as chronic diseases and certain pathological conditions.
Used in Drug Development:
[(2-phenylquinolin-4-yl)sulfanyl]acetic acid [(2-phenylquinolin-4-yl)sulfanyl]acetic acid is also used in drug development to explore its potential as a therapeutic agent. Further research is necessary to fully understand its properties and possible applications, which may lead to the discovery of new treatments for various health issues.
Used in Antioxidant Applications:
[(2-phenylquinolin-4-yl)sulfanyl]acetic acid is used as an antioxidant agent for its ability to combat oxidative stress, which is a significant factor in the development of numerous diseases and conditions. Its antioxidant properties make it a potential candidate for the development of treatments aimed at reducing oxidative damage in the body.
Used in Anti-inflammatory Applications:
As an anti-inflammatory agent, [(2-phenylquinolin-4-yl)sulfanyl]acetic acid is used to address conditions characterized by inflammation, such as autoimmune disorders and chronic inflammatory diseases. Its potential to modulate inflammatory responses could lead to the development of new therapeutic strategies for these conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 5443-03-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5443-03:
(6*5)+(5*4)+(4*4)+(3*3)+(2*0)+(1*3)=78
78 % 10 = 8
So 5443-03-8 is a valid CAS Registry Number.

5443-03-8SDS

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 2-(2-phenylquinolin-4-yl)sulfanylacetic acid,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-(2-PHENYLQUINOLIN-4-YL)SULFANYLACETIC ACID HYDROCHLORIDE

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:5443-03-8 SDS

5443-03-8Upstream product

5443-03-8Downstream Products

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