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2-Ethoxyethyl chloroacetate, an organic chemical compound with the molecular formula C6H11ClO3, is a clear, colorless liquid characterized by a fruity odor. It serves as a versatile solvent and intermediate in the synthesis of various compounds, including pharmaceuticals and agrochemicals. Classified as a moderately hazardous chemical, it requires careful handling and the use of appropriate personal protective equipment to prevent skin, eye, and respiratory irritation.

60682-94-2

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60682-94-2 Usage

Uses

Used in Chemical Synthesis:
2-Ethoxyethyl chloroacetate is used as a solvent and intermediate for the synthesis of other compounds, facilitating the production of a wide range of chemical products.
Used in Pharmaceutical Industry:
2-Ethoxyethyl chloroacetate is used as a key component in the synthesis of pharmaceuticals, contributing to the development of new medications and therapeutic agents.
Used in Agrochemical Industry:
2-Ethoxyethyl chloroacetate is utilized as a precursor in the production of agrochemicals, such as pesticides and herbicides, to enhance crop protection and yield.
Used in Research and Development:
2-Ethoxyethyl chloroacetate is employed as a reagent in research and development laboratories, enabling the exploration of new chemical reactions and the discovery of novel compounds with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 60682-94-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,8 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60682-94:
(7*6)+(6*0)+(5*6)+(4*8)+(3*2)+(2*9)+(1*4)=132
132 % 10 = 2
So 60682-94-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H11ClO3/c1-2-9-3-4-10-6(8)5-7/h2-5H2,1H3

60682-94-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethoxyethyl 2-chloroacetate

1.2 Other means of identification

Product number -
Other names 2-Ethoxyethyl chloroacetate

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:60682-94-2 SDS

60682-94-2Relevant academic research and scientific papers

PHASE TRANSFER CATALYSED N-SUBSTITUTION OF 2H-1,2-BENZISOTHIAZOLIN-3-ONE 1,1-DIOXIDE

Svoboda, Jiri,Palecek, Jaroslav,Dedek, Vaclav

, p. 1304 - 1310 (2007/10/02)

The title compound on reaction with alkylating reagents and under the conditions of phase catalysis affords 2-substituted 2H-1,2-benzisothiazolin-3-one 1,1-dioxides (III).The conditions of the reaction and the mass spectra of the products are discussed.

PERFLUORINATED RESINSULFONIC ACID - A CATALYST FOR CERTAIN ORGANIC REACTIONS.

Etlis,Beshenova,Semenova,Shomina,Dreiman,Balaev

, p. 551 - 555 (2007/10/02)

The purpose of this work was to examine the possibility of using, as a catalyst in certain organic reactions, the perfluorinated resinsulfonic acid F-4SK in the H form, which is an analog of the perfluorinated resinsulfonic acid Nafion-H. To compare catalyst activity of the perfluorinated resinsulfonic acid in decomposition of cumene hydroperoxide, CHP was also decomposed in presence of KU-2 resin. It was found that during repeated use over a period of 150 h the activity of KU-2 catalyst under analogous conditions fell by 4-6%. During the same time the activity of the perfluorinated resinsulfonic acid remained unchanged. It is also known that the presence of a strong acid in the reaction mixture causes formation of by-products, namely the products of condensation of phenol with acetone and dimethylphenylcarbinol, and of dehydration of dimethylphenylcarbinol, with formation of alpha -methylstyrene and products of greater complexity.

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