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1,1,1-Trifluoro-2-trifluoromethyl-2-hydroxy-4-pentyl acrylate
[CAS# 859856-64-7]

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Identification
Name 1,1,1-Trifluoro-2-trifluoromethyl-2-hydroxy-4-pentyl acrylate
Synonyms [5,5,5-trifluoro-4-hydroxy-4-(trifluoromethyl)pentan-2-yl] prop-2-enoate
Molecular Structure CAS # 859856-64-7, 1,1,1-Trifluoro-2-trifluoromethyl-2-hydroxy-4-pentyl acrylate, [5,5,5-trifluoro-4-hydroxy-4-(trifluoromethyl)pentan-2-yl] prop-2-enoate
Molecular Formula C9H10F6O3
Molecular Weight 280.16
CAS Registry Number 859856-64-7
SMILES CC(CC(C(F)(F)F)(C(F)(F)F)O)OC(=O)C=C
up Discovory and Applicatios
1,1,1-Trifluoro-2-trifluoromethyl-2-hydroxy-4-pentyl acrylate is a fluorinated acrylate derivative, a special class of chemical compounds. The exploration of fluorinated acrylates began in the mid-20th century in search of materials with excellent chemical resistance and hydrophobicity. 1,1,1-Trifluoro-2-trifluoromethyl-2-hydroxy-4-pentyl acrylate was developed by integrating the trifluoromethyl group into the acrylate framework. This was due to the need for high-performance materials that can withstand harsh environments and provide functional surfaces.

The structure of the compound consists of a fluorinated acrylate backbone, hydroxyl and pentyl side chains. Fluorination provides chemical resistance and hydrophobicity. The acrylate portion promotes polymerization, resulting in a cross-linked network and functional materials.

The compound is used to produce fluorinated polymers that can be used in protective coatings. These coatings are resistant to solvents, acids, and bases, making them suitable for use in harsh environments. Polymers derived from this acrylate can be used to create hydrophobic surfaces that repel water and reduce surface contamination, which is very beneficial for applications such as antifouling coatings and self-cleaning materials.

This compound is used to synthesize dielectric materials for electronic applications. Its properties improve the performance and reliability of components such as capacitors and printed circuit boards. Fluorinated polymers made from this acrylate provide encapsulation for sensitive electronic components, protecting them from moisture and chemicals.

It can also be used to create biocompatible coatings for medical devices and implants, where chemical resistance and low friction are critical. The properties of this compound can be used to develop controlled-release, stable drug delivery systems in biological environments.

Used in coatings in aerospace applications, this compound resists extreme temperatures and corrosive environments, helping to extend the service life and reliability of aircraft components. It enhances the performance of composites used in aerospace by providing a durable, lightweight and chemical-resistant surface.
Market Analysis Reports
List of Reports Available for 1,1,1-Trifluoro-2-trifluoromethyl-2-hydroxy-4-pentyl acrylate
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