14258-40-3

Basic information

• Product Name: 2-(2-Chloro ethoxy) Ethyl acetate
• Synonyms: ethyl 2-(2-chloroethoxy)acetate;NSC 72730;Ethanol,2-(2-chloroethoxy)-, 1-acetate;2-(2-Chloroethoxy)ethanol acetate
• CAS NO: 14258-40-3
• Molecular Formula: C₆H₁₁ClO₃
• Molecular Weight: 166.60
• Mol File: 14258-40-3.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 223℃
• Flash Point: 92℃
• Appearance: /
• Density: 1.119
• Vapor Pressure: 0.1mmHg at 25°C
• Refractive Index: 1.427
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 2-(2-Chloro ethoxy) Ethyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-Chloro ethoxy) Ethyl acetate(14258-40-3)
• EPA Substance Registry System: 2-(2-Chloro ethoxy) Ethyl acetate(14258-40-3)

Safety Data

• Hazardous Substances Data: 14258-40-3(Hazardous Substances Data)

Usage

Description

2-(2-Chloro ethoxy) Ethyl acetate, with the molecular formula C6H11ClO3, is a clear, colorless liquid characterized by a faint characteristic odor. It is a versatile chemical compound that serves as a solvent in a variety of applications due to its unique properties.

Uses

Used in Coatings and Paints Industry:
2-(2-Chloro ethoxy) Ethyl acetate is used as a solvent to dissolve and mix various components in coatings and paints, enhancing their performance and application characteristics.
Used in Inks Industry:
In the ink industry, 2-(2-Chloro ethoxy) Ethyl acetate is utilized as a solvent to improve the flow and consistency of inks, ensuring high-quality printing and even distribution of color.
Used in Adhesives Industry:
As a component in adhesive formulations, 2-(2-Chloro ethoxy) Ethyl acetate is used to adjust the viscosity and bonding properties of adhesives, contributing to their effectiveness in various applications.
Used in Cleaning Agents:
2-(2-Chloro ethoxy) Ethyl acetate is employed as an active ingredient in cleaning agents, where it helps dissolve and remove dirt, grease, and other contaminants.
Used in Pharmaceutical Production:
In the pharmaceutical sector, 2-(2-Chloro ethoxy) Ethyl acetate is used as a solvent in the synthesis of various drugs, facilitating chemical reactions and improving the yield of desired products.
Used in Agrochemicals Production:
2-(2-Chloro ethoxy) Ethyl acetate is also utilized in the production of agrochemicals, where it serves as a solvent for the synthesis of pesticides and other agricultural chemicals, enhancing their effectiveness and performance.
Despite its low toxicity, it is crucial to adhere to proper handling and storage procedures to prevent any potential health or environmental risks associated with 2-(2-Chloro ethoxy) Ethyl acetate.

InChI:InChI=1/C6H11ClO3/c1-6(8)10-5-4-9-3-2-7/h2-5H2,1H3

Upstream product

• 108-24-7 acetic anhydride 
• 628-89-7 2-(2-Chloroethoxy)ethanol 
• 163193-79-1 4-nitrobenzyl 2,2,2-trichloroethanimidoate 
• 64-19-7 acetic acid 
• 41489-83-2 1,1-bis<2-(2-chloroethoxy)ethoxy>ethane 
• 123-91-1 1,4-dioxane 
• 75-36-5 acetyl chloride 
• 127-09-3 sodium acetate 
• 111-44-4 3-oxa-1,5-dichloropentane 

Downstream Products

• 3603-43-8 2-(2-piperidin-1-yl-ethoxy)-ethanol 
• 628-89-7 2-(2-Chloroethoxy)ethanol 
• 3603-45-0 4-(2(2-hydroxyethoxy)ethyl)-morpholine 
• 1274686-40-6 4-(Z-N-2-aminoethanamido)-N₁,N₇-bis[2-(2-acetoxyethoxy)ethyl]-4-{3-[2-(2-acetoxyethoxy)ethylamino]-3-oxopropyl}heptanediamide 
• 20427-84-3 nonoxynol-9 
• 140-82-9 2-[2-(diethylamino)ethoxy] ethanol 

Relevant articles and documents

A Family of Amphiphilic Cyclodextrin Liquid Crystals Governed by Dipole–Dipole Interactions

A novel family of amphiphilic cyclodextrin(CD)-based liquid crystals that bear O-acetylated oligoethylene glycol chains at the secondary face is reported. Unlike most of the previously reported liquid crystals (LC) based on chemically modified CDs, which depend on H-bonding as the primary intermolecular forces, the present CD derivatives self-assemble into highly ordered smectic liquid crystal phases via the weaker dipole–dipole intermolecular interactions. The obtained materials are found to display much improved properties such as improved thermostability, reduced clearing temperatures, and better fluidity. The present work opens up new possibilities to design CD-based LC materials.

Synthesis Toward and Stereochemical Assignment of Clathsterol: Exploring Diverse Strategies to Polyoxygenated Sterols

Herein we describe a synthesis of the trisulfate derivative of clathsterol (1), a marine sterol endowed with impressive structural features and moderate inhibitory activity against HIV-1 reverse transcriptase. By synthesizing two possible isomers of the side chain, the stereochemistry of 1 is assigned. In creating chiral side chains from steroidal lactone, our strategies, including an addition/reduction procedure to give C22R-OH, an epoxide-opening reaction, and a [3.3]-rearrangement to induce the generation of C24S-Et and C24R-Et respectively, are highly flexible and complementary to each other.

HYDANTOIN CONTAINING DEOXYURIDINE TRIPHOSPHATASE INHIBITORS

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