89124-14-1

Basic information

• Product Name: [(2-chloroethyl)sulfanyl]acetyl chloride
• CAS NO: 89124-14-1
• Molecular Formula: C₄H₆Cl₂OS
• Molecular Weight: 173.0608
• Mol File: 89124-14-1.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 223.8°C at 760 mmHg
• Flash Point: 89.1°C
• Density: 1.347g/cm³
• Vapor Pressure: 0.0946mmHg at 25°C
• Refractive Index: 1.508
• CAS DataBase Reference: [(2-chloroethyl)sulfanyl]acetyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: [(2-chloroethyl)sulfanyl]acetyl chloride(89124-14-1)
• EPA Substance Registry System: [(2-chloroethyl)sulfanyl]acetyl chloride(89124-14-1)

Safety Data

• Hazardous Substances Data: 89124-14-1(Hazardous Substances Data)

Usage

Description

[(2-chloroethyl)sulfanyl]acetyl chloride, also known as S-2-(2-chloroethylthio)acetyl chloride, is a chloroethyl thioester with the chemical formula C4H6Cl2O2S. It is a colorless to light yellow liquid with a characteristic odor and is recognized for its role as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, it serves as a reagent in organic synthesis for introducing the acetylthio group into molecules. Given its potential hazards, including corrosiveness and harmful effects upon inhalation or ingestion, it requires careful handling and appropriate safety measures in a controlled laboratory environment.

Uses

Used in Pharmaceutical Synthesis:
[(2-chloroethyl)sulfanyl]acetyl chloride is used as an intermediate for the production of various pharmaceuticals. Its application is crucial in the development of new drugs and medicines, contributing to the advancement of the pharmaceutical industry.
Used in Agrochemical Synthesis:
In the agrochemical industry, [(2-chloroethyl)sulfanyl]acetyl chloride is utilized as an intermediate in the synthesis of different agrochemicals. This involvement is essential for the creation of products that can enhance crop protection and contribute to increased agricultural productivity.
Used as a Reagent in Organic Synthesis:
[(2-chloroethyl)sulfanyl]acetyl chloride is employed as a reagent in organic synthesis to introduce the acetylthio group into molecules. This function is vital for the modification and enhancement of molecular structures, leading to the development of novel compounds with specific properties and applications across various industries.