4513-42-2

Basic information

• Product Name: 2,4-dichlorophenoxy acrylate
• Synonyms: 2,4-dichlorophenoxy acrylate
• CAS NO: 4513-42-2
• Molecular Weight: 217.051
• Mol File: 4513-42-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2,4-dichlorophenoxy acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-dichlorophenoxy acrylate(4513-42-2)
• EPA Substance Registry System: 2,4-dichlorophenoxy acrylate(4513-42-2)

Safety Data

• Hazardous Substances Data: 4513-42-2(Hazardous Substances Data)

Usage

General Description

2,4-dichlorophenoxy acrylate is a chemical compound that is derived from 2,4-dichlorophenoxyacetic acid (2,4-D), a commonly used herbicide. It is used as a herbicide itself, and is often employed to control broadleaf weeds in various agricultural and horticultural settings. The compound works by disrupting the growth of plants and inhibiting their ability to produce certain essential proteins, ultimately leading to their death. Due to its effectiveness as a herbicide, 2,4-dichlorophenoxy acrylate is widely used in both commercial and residential settings, although concerns have been raised about its potential environmental and health impacts. It is important for users of this chemical to adhere to safety regulations and guidelines to minimize any potential risks.

Upstream product

• 814-68-6 acryloyl chloride 
• 120-83-2 2,4-dichlorophenol 
• 79-10-7 acrylic acid 

Relevant articles and documents

Tandem type polymerization. Synthesis and characterization of ordered poly(amide-thioether) from 2,6-dichlorophenyl methacrylate, 4,4′-thiobis(benznenethiol), and 4,4′-oxydianiline

Ordered poly(amide-thioether) (17) was prepared by tandem type polymerization of 2,4-dichlorophenyl acrylate (11), 4,4′-thiobis(benznenthiol) (12), and 4,4′-oxydianiline (16). The polymerization was carried out by mixing all monomers in the presence of catalytic amounts of triethylamine (TEA) and 1-hydroxybenzotriazole (HOBt) in 1-methyl-2-pyrrolidinone (NMP) at 20 °C for 2 h and then 80 °C for 2 days, yielding polymer 17 with a number-average molecular weight (Mn) of 25 000. Authentic ordered poly(amide-thioether) (18) was prepared to verify the structure of polymer 17. The microstructure of polymers obtained was investigated by 1H and 13C NMR spectroscopy, and it has been found the polymer obtained has the expected ordered structure. Furthermore, model reactions were studied in detail to demonstrate the feasibility of ordered polymer formation.

SUBSTITUTED BENZOHYDRAZIDE ANALOGS AS HISTONE DEMETHYLASE INHIBITORS

Benzohydrazide analogs, derivatives thereof, and related compounds, which are useful as inhibitors of lysine-specific histone demethyfase, including LSD1 and LSD2; synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of using the compounds and compositions to treat disorders associated with dysfunction of the LSD1 and/or LSD2.

FURTHER STUDY OF ESTERTIN TRICHLORIDES, Cl3SnCH2CH2CO2R. LEWIS ACIDITY TOWARDS ACETONITRILE. CRYSTAL STRUCTURE OF Cl3SnCH2CH2CO2Pr-i

Crystals of Cl3SnCH2CH2CO2Pr-i are orthorombic, space group P212121 with a 9.638(6), b 10.004(7) and c 12.848(8) Angstroem.The tin atom is five-coordinate with two chlorines and carbon equatorial and the remaining chlorine and the carbonyl oxygen axial, in a distorted trigonal-bipyramidal arrangement: (Sn-Cl)ax 2.389(3), average (Sn-Cl)eq 2.320(2), Sn-C 2.142(9), Sn-O 2.337(5) Angstroem.Apart from the equatorial chlorine and the terminal carbons in the isopropyl group, all non-hydrogen atoms are essentially coplanar.The molecule approaches C2v symmetry although not constrained to do so by the crystallographic space group.In MeCN solution, the compounds Cl3SnCH2CH2CO2R (I, R = Me, Pr-i, C6H4X (X = p-MeO, H, p-Cl, o-MeO) or C6H3Cl2-2,4) form as equilibrium mixtures of 1/1 and 2/1 MeCN/1 complexes; the chelate ring is broken in the 2/1 complexes.Equilibrium constants indicate that the strength of the intramolecular Sn-O coordination I increases with the electron releasing ability of the R group.