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14258-40-3

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14258-40-3 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.

Check Digit Verification of cas no

The CAS Registry Mumber 14258-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,5 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14258-40:
(7*1)+(6*4)+(5*2)+(4*5)+(3*8)+(2*4)+(1*0)=93
93 % 10 = 3
So 14258-40-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H11ClO3/c1-6(8)10-5-4-9-3-2-7/h2-5H2,1H3

14258-40-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-Chloro ethoxy) Ethyl acetate

1.2 Other means of identification

Product number -
Other names 2-(2-Chloroethoxy)ethyl acetate

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:14258-40-3 SDS

14258-40-3Relevant articles and documents

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

Champagne, Pier-Luc,Ester, David,Ward, Sandra,Williams, Vance E.,Ling, Chang-Chun

, p. 423 - 432 (2017)

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

Zhou, Tao,Feng, Feng,Shi, Yong,Tian, Wei-Sheng

, p. 2308 - 2311 (2016)

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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Paragraph 0927, (2018/06/12)

Provided herein are dUTPase inhibitors, compositions comprising such compounds and methods of using such compounds and compositions.

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