To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

How to transfigure the Wikipedia

Would you like Wikipedia to always look as professional and up-to-date? We have created a browser extension. It will enhance any encyclopedic page you visit with the magic of the WIKI 2 technology.

Try it — you can delete it anytime.

Install in 5 seconds
4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
Great Wikipedia has got greater.
.
Leo
Newton
Brights
Milds

Ethyl chloroacetate

From Wikipedia, the free encyclopedia

Ethyl chloroacetate
Names
Preferred IUPAC name
Ethyl chloroacetate
Other names
  • Ethyl 2-chloroacetate
  • Ethyl monochloroacetate
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.002.995 Edit this at Wikidata
EC Number
  • 203-294-0
UNII
UN number 1181
  • InChI=1S/C4H7ClO2/c1-2-7-4(6)3-5/h2-3H2,1H3
    Key: VEUUMBGHMNQHGO-UHFFFAOYSA-N
  • InChI=1/C4H7ClO2/c1-2-7-4(6)3-5/h2-3H2,1H3
    Key: VEUUMBGHMNQHGO-UHFFFAOYAS
  • ClCC(=O)OCC
Properties
ClCH2CO2CH2CH3
Molar mass 122.55 g·mol−1
Density 1.145 g/mL[1]
Melting point −26 °C (−15 °F; 247 K)[1]
Boiling point 143 °C (289 °F; 416 K)[1]
−72.3·10−6 cm3/mol
Hazards
GHS labelling:[2]
GHS06: Toxic
GHS09: Environmental hazard
Danger
H301, H311, H331, H400
P261, P262, P264, P270, P271, P273, P280, P301+P316, P302+P352, P304+P340, P316, P321, P330, P361+P364, P391, P403+P233, P405, P501
Related compounds
Related esters
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Ethyl chloroacetate is an organic compound with the chemical formula ClCH2CO2CH2CH3. It is used primarily in the chemical industry. It is used as a solvent for organic synthesis and as an intermediate in the production of pesticides (such as sodium fluoroacetate).[3]

An example for the use of this agent was in the synthesis of cinepazet.

YouTube Encyclopedic

  • 1/3
    Views:
    1 565
    7 255
    2 407
  • Ethyl chloroacetate preparation
  • Ethyl iodide using iodine and aluminium foil
  • Diethylmalonate synthesis from chloroacetic acid

Transcription

References

  1. ^ a b c Ethyl chloroacetate at Sigma-Aldrich
  2. ^ "Ethyl chloroacetate". pubchem.ncbi.nlm.nih.gov.
  3. ^ "Ethyl chloroacetate" (PDF). U.S. Environmental Protection Agency. April 2009.[permanent dead link]


Stub icon

This article about an organic halide is a stub. You can help Wikipedia by expanding it.

This page was last edited on 15 April 2024, at 21:51
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.
Contact WIKI 2
Introduction
Terms of Service
Privacy Policy