144261-43-8

Basic information

• Product Name: 2-Propenoic acid, [4-(trifluoromethyl)phenyl]methyl ester
• CAS NO: 144261-43-8
• Molecular Formula: C11H9F3O2
• Molecular Weight: 230.186
• Mol File: 144261-43-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-Propenoic acid, [4-(trifluoromethyl)phenyl]methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoic acid, [4-(trifluoromethyl)phenyl]methyl ester(144261-43-8)
• EPA Substance Registry System: 2-Propenoic acid, [4-(trifluoromethyl)phenyl]methyl ester(144261-43-8)

Safety Data

• Hazardous Substances Data: 144261-43-8(Hazardous Substances Data)

Usage

General Description

2-Propenoic acid, [4-(trifluoromethyl)phenyl]methyl ester is a chemical compound that belongs to the class of acrylate esters. It is a colorless liquid that is commonly used as a monomer in the production of polymers and resins. 2-Propenoic acid, [4-(trifluoromethyl)phenyl]methyl ester has the molecular formula C11H9F3O2 and a molecular weight of 232.18 g/mol. It is primarily used as a chemical intermediate in the production of various products such as adhesives, coatings, and sealants. It is also used in the formulation of specialty chemicals and as a building block for the synthesis of other compounds in the chemical industry. Additionally, it has applications in the production of pharmaceuticals and agrochemicals. However, it is important to handle this compound with care and use appropriate safety measures due to its potential hazards.

Upstream product

• 79-10-7 acrylic acid 
• 402-49-3 4-bromomethyltrifluoromethylbenzene 
• 349-95-1 4-(trifluoromethyl)benzylic alcohol 
• 814-68-6 acryloyl chloride 

Downstream Products

• 144261-59-6 3-phenyl-3-hydroxy-2-methylene-propanoic acid p-trifluoromethylbenzyl ester 

Relevant articles and documents

Modification and chemical transformation of Si(1 1 1) surface

Modification of hydrogen-terminated Si(1 1 1) surfaces by hydrosilylation of activated alkenes and further chemical transformation of the modified surfaces is reported. A Si(1 1 1)-H surface was reacted with activated alkenes such as acrylate esters, acry

Asymmetric Michael addition of malonic diesters to acrylates by phase-transfer catalysis toward the construction of quaternary stereogenic α-carbons

A highly enantioselective construction of an all-carbon quaternary stereogenic center at the α-position of malonic diesters has been achieved by Michael addition using phase-transfer catalysis. The reaction of α-monosubstituted malonates with acrylates in

The 'Baylis - Hillman reaction' mechanism and applications revisited

It is shown that reaction of aryl, benzyl, alkyl and functionalised alkyl acrylic esters with benzaldehyde, in the presence of 1,4-diazabicyclo[2.2.2] octane, strongly depends upon the electronic and steric effects of the ester part. This influence is also observed in condensation of furfuraldehyde. Moreover, for the first time, it is shown that the overall condensation is equilibrated.