1464-69-3

  • Product Name:2-(vinyloxy)ethyl methacrylate
  • Molecular Formula:C8H12 O3
  • Molecular Weight:156.181
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Product Details

Purity:99%

Factory Sells Best Quality 2-(vinyloxy)ethyl methacrylate 1464-69-3 with steady supply

  • Molecular Formula:C8H12 O3
  • Molecular Weight:156.181
  • Vapor Pressure:0.265mmHg at 25°C 
  • Refractive Index:1.4430 (estimate) 
  • Boiling Point:204.4°C at 760 mmHg 
  • Flash Point:76.7°C 
  • PSA:35.53000 
  • Density:0.973g/cm3 
  • LogP:1.26580 

2-(vinyloxy)ethyl methacrylate(Cas 1464-69-3) Usage

General Description

2-(vinyloxy)ethyl methacrylate is a chemical compound that is used in the production of various polymers and coatings. It is a clear, colorless liquid with a sweet, fruity odor, and is highly flammable. This chemical is commonly used as a monomer in the formation of polymeric materials such as adhesives, paints, and sealants. 2-(vinyloxy)ethyl methacrylate is also known for its ability to improve the adhesion and durability of coatings, as well as its resistance to chemicals and weathering. It is important to handle this chemical with care, as it can cause irritation to the skin and eyes, and can be harmful if ingested or inhaled.

InChI:InChI=1/C8H12O3/c1-4-10-5-6-11-8(9)7(2)3/h4H,1-2,5-6H2,3H3

1464-69-3 Relevant articles

Fabrication of Acidic pH-Cleavable Polymer for Anticancer Drug Delivery Using a Dual Functional Monomer

Zheng, Luping,Zhang, Xiaolong,Wang, Yunfei,Liu, Fangjun,Peng, Jinlei,Zhao, Xuezhi,Yang, Huiru,Ma, Liwei,Wang, Baoyan,Chang, Cong,Wei, Hua

, p. 3874 - 3882 (2018)

The preparation of tumor acidic pH-cleav...

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Haas,Simon

, p. 421 (1957)

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Photoresist resin monomer synthesized from carboxylic acid compound and synthesis method thereof

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Paragraph 0033; 0035-0037, (2020/05/14)

The invention discloses a photoresist re...

Acid-responsive cross-linked polymer prodrug, and preparation method and application thereof

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Paragraph 0068-0072, (2020/07/15)

The invention discloses an acid-responsi...

SALT, ACID GENERATOR, RESIN, RESIST COMPOSITION AND METHOD FOR PRODUCING RESIST PATTERN

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Paragraph 0691; 0692, (2016/12/01)

A salt represented by formula (I): where...

1464-69-3 Process route

ethyleneglycol vinyl ether
764-48-7

ethyleneglycol vinyl ether

Methacryloyl chloride
920-46-7,26937-45-1

Methacryloyl chloride

2-(vinyloxy)ethyl methacrylate
1464-69-3

2-(vinyloxy)ethyl methacrylate

Conditions
Conditions Yield
With triethylamine; In dichloromethane; at 0 - 20 ℃; for 4.5h; Inert atmosphere;
84%
With triethylamine; In dichloromethane; at 0 - 20 ℃; for 4.5h; Inert atmosphere;
80.3%
With triethylamine; In diethyl ether; at 10 ℃;
65%
With pyridine; In diethyl ether; at 35 ℃; for 4h;
60%
With triethylamine; In dichloromethane; at 20 ℃; for 8h;
51.6%
With pyridine; diethyl ether;
ethyleneglycol vinyl ether; With triethylamine; In tetrahydrofuran; at 23 ℃; for 0.5h;
Methacryloyl chloride; In tetrahydrofuran; at 0 ℃; for 1.5h;
ethyleneglycol vinyl ether; With triethylamine; In tetrahydrofuran; at 23 ℃; for 0.5h;
Methacryloyl chloride; In tetrahydrofuran; at 0 ℃; for 1.5h;
ethyleneglycol vinyl ether
764-48-7

ethyleneglycol vinyl ether

methacrylic acid methyl ester
80-62-6,114512-63-9,143476-91-9,25188-98-1,9011-14-7

methacrylic acid methyl ester

2-(vinyloxy)ethyl methacrylate
1464-69-3

2-(vinyloxy)ethyl methacrylate

Conditions
Conditions Yield
With sodium 2-vinyloxyethoxide; N-Phenyl-2-naphthylamine; hydroquinone; at 95 ℃; for 4h; Product distribution; other basic reagents;
93.3 % Turnov.
With sodium 2-vinyloxyethoxide; N-Phenyl-2-naphthylamine; hydroquinone; at 95 ℃; for 4h;
93.3 % Turnov.
With 10H-phenothiazine; ethylene glycol divinyl ether; dioctyltin(IV) oxide; at 130 ℃; for 8h;
With 10H-phenothiazine; oxygen; di(n-butyl)tin oxide;
With 10H-phenothiazine; di(n-butyl)tin oxide; In water;
With methoxyhydroquinone; oxygen; di(n-butyl)tin oxide;
With 2-methyl-1,3-dioxolane; 10H-phenothiazine; ethylene glycol divinyl ether; dioctyltin(IV) oxide; at 130 ℃; for 7.5h;
With 2-methyl-1,3-dioxolane; 10H-phenothiazine; dioctyltin(IV) oxide; at 130 ℃; for 8h;
With 10H-phenothiazine; dioctyltin(IV) oxide; for 11h;
With methanol; sodium methylate;

1464-69-3 Upstream products

  • 764-48-7
    764-48-7

    ethyleneglycol vinyl ether

  • 80-62-6
    80-62-6

    methacrylic acid methyl ester

  • 97-88-1
    97-88-1

    2-methyl-butyl acrylate

  • 920-46-7
    920-46-7

    Methacryloyl chloride

1464-69-3 Downstream products

  • 534-15-6
    534-15-6

    1,1-dimethoxyethane