51-68-3

  • Product Name:2-(Dimethylamino)ethyl (4-chlorphenoxy)acetate
  • Molecular Formula:C12H16ClNO3
  • Purity:99%
  • Molecular Weight:257.717
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Product Details;

CasNo: 51-68-3

Molecular Formula: C12H16ClNO3

Reliable Factory Supply  Quality 2-(Dimethylamino)ethyl (4-chlorphenoxy)acetate 51-68-3 with Safe Shipping

  • Molecular Formula:C12H16ClNO3
  • Molecular Weight:257.717
  • Vapor Pressure:5.95E-05mmHg at 25°C 
  • Melting Point:138-140 °C 
  • Refractive Index:1.52 
  • Boiling Point:345.941 °C at 760 mmHg 
  • PKA:8.17±0.28(Predicted) 
  • Flash Point:163.019 °C 
  • PSA:38.77000 
  • Density:1.179 g/cm3 
  • LogP:1.82360 

2-(Dimethylamino)ethyl (4-chlorphenoxy)acetate(Cas 51-68-3) Usage

Use Description

2-(Dimethylamino)ethyl (4-chlorophenoxy)acetate is a chemical compound with diverse applications in different fields. In the agrochemical industry, it serves as a key ingredient in the formulation of herbicides, contributing to weed control in agriculture. Its role is vital in protecting crops and improving agricultural yields. Additionally, in the pharmaceutical sector, this compound can be employed as an intermediate in the synthesis of pharmaceuticals and organic molecules, offering versatility in drug discovery and development. Moreover, in academic research and organic chemistry, it functions as a building block for the creation of complex molecules, facilitating studies in chemical synthesis and the exploration of new chemical reactions. Its multifaceted applications highlight its significance in agriculture, pharmaceuticals, and chemical research, contributing to crop protection, drug development, and the advancement of chemical science.

Consumer Uses

ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment.

InChI:InChI=1/C12H16ClNO3/c1-14(2)7-8-16-12(15)9-17-11-5-3-10(13)4-6-11/h3-6H,7-9H2,1-2H3

51-68-3 Relevant articles

Chlorination Reaction of Aromatic Compounds and Unsaturated Carbon-Carbon Bonds with Chlorine on Demand

Liu, Feng,Wu, Na,Cheng, Xu

supporting information, p. 3015 - 3020 (2021/05/05)

Chlorination with chlorine is straightfo...

Esterquat herbicidal ionic liquids (HILs) with two different herbicides: Evaluation of activity and phytotoxicity

Syguda, Anna,Gielnik, Anna,Borkowski, Andrzej,Wo?niak-Karczewska, Marta,Parus, Anna,Piechalak, Aneta,Olejnik, Anna,Marecik, Roman,?awniczak, ?ukasz,Chrzanowski, ?ukasz

supporting information, p. 9819 - 9827 (2018/06/18)

Herbicidal ionic liquids (HILs) constitu...

POTENTIAL CEREBRAL STIMULANTS: ESTERS OF 2-DIMETHYLAMINOETHANOL WITH SOME LIPOPHILIC CARBOXYLIC ACIDS

Protiva, Miroslav,Valenta, Vladimir,Kopicova, Zdenka,Lukac, Juraj,Holubek, Jiri,Krejci, Ivan

, p. 1278 - 1289 (2007/10/02)

2-Dimethylaminoethyl esters of 2,2-dimet...

51-68-3 Process route

2-(dimethylamino)ethyl phenoxyacetate
50837-15-5

2-(dimethylamino)ethyl phenoxyacetate

meclofenoxate
51-68-3

meclofenoxate

Conditions
Conditions Yield
With tetraethylammonium chloride; trichloroacetonitrile; In acetonitrile; at 23 ℃; for 2h; Electrochemical reaction; Inert atmosphere;
52%
meclofenoxate hydrochloride
3685-84-5

meclofenoxate hydrochloride

meclofenoxate
51-68-3

meclofenoxate

Conditions
Conditions Yield
With triethylamine; In chloroform;
78%

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