2-(2-(2-Methoxyethoxy)ethoxy)ethyl methacrylate - 24493-59-2

2-(2-(2-Methoxyethoxy)ethoxy)ethyl methacrylate

Catalog Number: EVT-313712
CAS Number: 24493-59-2
Molecular Formula: C11H20O5
Molecular Weight: 232.27 g/mol
The product is for non-human research only. Not for therapeutic or veterinary use.
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Product Introduction

Description
2-(2-(2-Methoxyethoxy)ethoxy)ethyl methacrylate, also known as MEO2MA, is a monomer used in the production of various polymers and copolymers. It is a colorless liquid with a molecular weight of 218.26 g/mol and a boiling point of 160-162°C. MEO2MA is widely used in medical, environmental, and industrial research due to its unique chemical structure and biological activity.
Applications in Various Fields
2-(2-(2-Methoxyethoxy)ethoxy)ethyl methacrylate has a wide range of applications in medical, environmental, and industrial research. In medical research, it is used in drug development and clinical trials to evaluate its efficacy and safety in treating various diseases. It has also been used in the production of medical devices and implants due to its biocompatibility and hydrophilic properties. In environmental research, 2-(2-(2-Methoxyethoxy)ethoxy)ethyl methacrylate is used to study its effects on ecosystems and its role in pollution management. In industrial research, it is used in manufacturing processes to improve product quality and efficiency. Health and safety considerations should be taken into account when using 2-(2-(2-Methoxyethoxy)ethoxy)ethyl methacrylate in these applications.

Properties

CAS Number

24493-59-2

Product Name

2-(2-(2-Methoxyethoxy)ethoxy)ethyl methacrylate

IUPAC Name

2-[2-(2-methoxyethoxy)ethoxy]ethyl 2-methylprop-2-enoate

Molecular Formula

C11H20O5

Molecular Weight

232.27 g/mol

InChI

InChI=1S/C11H20O5/c1-10(2)11(12)16-9-8-15-7-6-14-5-4-13-3/h1,4-9H2,2-3H3

InChI Key

OBBZSGOPJQSCNY-UHFFFAOYSA-N

SMILES

CC(=C)C(=O)OCCOCCOCCOC

Canonical SMILES

CC(=C)C(=O)OCCOCCOCCOC
Method of Synthesis or Extraction
2-(2-(2-Methoxyethoxy)ethoxy)ethyl methacrylate can be synthesized using various methods, including the reaction of methoxyethyl methacrylate with ethylene oxide, the reaction of methoxyethyl methacrylate with ethylene glycol, and the reaction of methoxyethyl methacrylate with ethylene carbonate. The efficiency and yield of each method vary depending on the reaction conditions and the purity of the starting materials. Environmental and safety considerations should also be taken into account during the synthesis process, as some of the reactants and by-products may be hazardous to human health and the environment.
Chemical Structure and Biological Activity
2-(2-(2-Methoxyethoxy)ethoxy)ethyl methacrylate contains a methacrylate group and three methoxyethyl groups, which make it highly reactive and hydrophilic. It can undergo polymerization and copolymerization reactions with various monomers to form polymers with unique properties. 2-(2-(2-Methoxyethoxy)ethoxy)ethyl methacrylate has been shown to exhibit biological activity by inhibiting the growth of cancer cells and reducing inflammation. Its mechanism of action and biological targets are still under investigation, but it is believed to interact with cellular signaling pathways and modulate gene expression.
Biological Effects
2-(2-(2-Methoxyethoxy)ethoxy)ethyl methacrylate has been shown to affect cell function and signal transduction by altering the expression of genes involved in cell growth, differentiation, and apoptosis. It has also been shown to have potential therapeutic effects in the treatment of cancer, inflammation, and other diseases. However, its toxic effects on human health and the environment are still unclear and require further investigation.
Future Perspectives and Challenges
The use and study of 2-(2-(2-Methoxyethoxy)ethoxy)ethyl methacrylate face several limitations, including its potential toxicity and environmental impact, as well as the need for further research to fully understand its biological activity and mechanism of action. Possible solutions and improvements include the development of safer and more sustainable synthesis methods, the use of alternative monomers with similar properties, and the optimization of its biological activity for therapeutic applications. Future trends and prospects in the application of 2-(2-(2-Methoxyethoxy)ethoxy)ethyl methacrylate in scientific research include its potential use in tissue engineering, drug delivery, and other biomedical applications.

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