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2-PHENOXYETHYL METHACRYLATE is a versatile chemical compound that is widely used in the production of polymers, coatings, specialty plastics, and adhesives. It is a clear liquid with a mild, sweet odor and is soluble in most organic solvents. Its unique properties, such as improving adhesion and flexibility in coatings, make it a valuable component in various industries.

10595-06-9

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10595-06-9 Usage

Uses

Used in Polymer and Coating Production:
2-PHENOXYETHYL METHACRYLATE is used as a monomer for the production of polymers and copolymers, enhancing the adhesion and flexibility of coatings. Its ability to improve the performance of coatings makes it a preferred choice in this application.
Used in Specialty Plastics and Adhesives Synthesis:
In the synthesis of specialty plastics and adhesives, 2-PHENOXYETHYL METHACRYLATE is used as a key component, contributing to the development of high-performance materials with specific properties tailored to various applications.
Used as a Chemical Intermediate:
2-PHENOXYETHYL METHACRYLATE also serves as a chemical intermediate in the production of other compounds, showcasing its versatility and importance in the chemical industry.
Overall, 2-PHENOXYETHYL METHACRYLATE is a valuable chemical compound with a wide range of applications across different industries, including polymer and coating production, specialty plastics and adhesives synthesis, and as a chemical intermediate. Its unique properties and versatility make it an essential component in the development of high-performance materials.

Check Digit Verification of cas no

The CAS Registry Mumber 10595-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,9 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10595-06:
(7*1)+(6*0)+(5*5)+(4*9)+(3*5)+(2*0)+(1*6)=89
89 % 10 = 9
So 10595-06-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O3/c1-9(2)12(13)15-10(3)14-11-7-5-4-6-8-11/h4-8,10H,1H2,2-3H3

10595-06-9 Well-known Company Product Price

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  • Aldrich

  • (458791)  Ethyleneglycolphenylethermethacrylate  contains 200 ppm monomethyl ether hydroquinone as inhibitor, 200 ppm hydroquinone as inhibitor

  • 10595-06-9

  • 458791-100ML

  • 697.32CNY

  • Detail
  • Aldrich

  • (458791)  Ethyleneglycolphenylethermethacrylate  contains 200 ppm monomethyl ether hydroquinone as inhibitor, 200 ppm hydroquinone as inhibitor

  • 10595-06-9

  • 458791-500ML

  • 2,543.58CNY

  • Detail

10595-06-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenoxyethyl 2-methylprop-2-enoate

1.2 Other means of identification

Product number -
Other names 2-Propenoic acid,2-methyl-,2-phenoxyethyl ester

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:10595-06-9 SDS

10595-06-9Relevant academic research and scientific papers

Method for synthesizing glycol phenyl ether methacrylate (by machine translation)

-

Paragraph 0030-0063, (2020/08/27)

Compared with a traditional esterification reaction, the ethylene glycol phenyl ether methacrylate has the advantages of being high in catalytic activity, less in side reaction, simple in post-treatment, free of waste water, small in environmental pollution and high in product yield, and belongs to the sustainable development green chemical engineering process. The method has the advantages of high catalytic activity, low side reaction, simple post-treatment, no wastewater generation, low environmental pollution and high yield. 94.44percent 91.36percent. (by machine translation)

Chemoselective Transesterification of Acrylate Derivatives for Functionalized Monomer Synthesis Using a Hard Zinc Alkoxide Generation Strategy

Nakatake, Daiki,Yazaki, Ryo,Ohshima, Takashi

supporting information, p. 3696 - 3699 (2016/08/20)

A new practical method for the synthesis of functionalized acrylate derivatives with the view to prepare functional polymers was explored. Hard zinc alkoxide generation enabled the highly chemoselective transesterification of acrylate derivatives over the undesired conjugate addition, which caused polymerization. The combined use of the catalytic zinc cluster Zn4(OCOCF3)6O and 4-(dimethylamino)pyridine delivered various functionalized acrylate derivatives through the transesterification of commercially available methyl acrylate derivatives with functionalized alcohols under mild conditions.

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