5443-01-6

Basic information

• Product Name: [(7-chloro-3-methylquinolin-4-yl)sulfanyl]acetic acid
• CAS NO: 5443-01-6
• Molecular Formula: C₁₂H₁₀ClNO₂S
• Molecular Weight: 267.7313
• Mol File: 5443-01-6.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 459.1°C at 760 mmHg
• Flash Point: 231.5°C
• Density: 1.44g/cm³
• Vapor Pressure: 3.18E-09mmHg at 25°C
• Refractive Index: 1.684
• CAS DataBase Reference: [(7-chloro-3-methylquinolin-4-yl)sulfanyl]acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: [(7-chloro-3-methylquinolin-4-yl)sulfanyl]acetic acid(5443-01-6)
• EPA Substance Registry System: [(7-chloro-3-methylquinolin-4-yl)sulfanyl]acetic acid(5443-01-6)

Safety Data

• Hazardous Substances Data: 5443-01-6(Hazardous Substances Data)

Usage

Description

[(7-chloro-3-methylquinolin-4-yl)sulfanyl]acetic acid is an organic compound characterized by its molecular formula C12H10ClNO2S. It features a quinoline ring with a chlorine atom and a methyl group attached, along with a thioether functional group connected to an acetic acid moiety. [(7-chloro-3-methylquinolin-4-yl)sulfanyl]acetic acid holds potential pharmacological and biological activities due to its sulfanyl group, which can engage in redox reactions and serve as a pharmacophore. Additionally, it may be utilized as a building block for synthesizing other organic compounds with unique characteristics and properties. Further research is necessary to fully comprehend its potential applications and effects.

Uses

Used in Pharmaceutical Industry:
[(7-chloro-3-methylquinolin-4-yl)sulfanyl]acetic acid is used as a potential pharmacological agent for its ability to participate in redox reactions and act as a pharmacophore. Its unique structure and properties make it a promising candidate for the development of new drugs targeting various diseases and conditions.
Used in Chemical Synthesis:
In the chemical industry, [(7-chloro-3-methylquinolin-4-yl)sulfanyl]acetic acid is used as a building block for the synthesis of other organic compounds with specific characteristics. Its versatile structure allows for the creation of a wide range of molecules with potential applications in various fields, including materials science, pharmaceuticals, and agrochemicals.
More research is required to explore the full potential of [(7-chloro-3-methylquinolin-4-yl)sulfanyl]acetic acid in different industries and applications. As our understanding of this compound grows, it may lead to the development of innovative products and therapies that can benefit society.

Upstream product

• 6622-28-2 4,7-dichloro-3-methylquinoline 
• 68-11-1 mercaptoacetic acid