728-47-2

Basic information

• Product Name: DiMethyl 4-(TrifluoroMethyl)phthalate
• Synonyms: DiMethyl 4-(TrifluoroMethyl)phthalate
• CAS NO: 728-47-2
• Molecular Formula: C₁₁H₉F₃O₄
• Molecular Weight: 262.1819696
• EINECS: -0
• Mol File: 728-47-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 270℃
• Flash Point: 114℃
• Appearance: /
• Density: 1.319
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: DiMethyl 4-(TrifluoroMethyl)phthalate(CAS DataBase Reference)
• NIST Chemistry Reference: DiMethyl 4-(TrifluoroMethyl)phthalate(728-47-2)
• EPA Substance Registry System: DiMethyl 4-(TrifluoroMethyl)phthalate(728-47-2)

Safety Data

• Hazardous Substances Data: 728-47-2(Hazardous Substances Data)

Usage

General Description

Dimethyl 4-(trifluoromethyl)phthalate is a chemical compound with the molecular formula C11H8F3O4. It is a colorless liquid that is commonly used as an intermediate in the synthesis of various organic compounds. This chemical is often utilized as a building block in the production of polymers, resins, and other industrial chemicals. Dimethyl 4-(trifluoromethyl)phthalate is known for its high stability and resistance to degradation, making it a valuable component in numerous manufacturing processes. However, it is important to handle this substance with caution, as it may possess potential risks to human health and the environment if not properly managed.

Upstream product

• 762-42-5 dimethyl acetylenedicarboxylate 
• 455941-77-2 (E)-1-ethoxy-3-trifluoromethyl-1,3-butadiene 
• 1984-43-6 dimethyl 7-oxabicyclo[2.2.1]hept-5-ene exo,exo-2,3-dicarboxylate 

Relevant articles and documents

Preparations of SF5- and CF3-substituted arenes utilizing the 7-oxabicyclo[2.2.1]hept-2-ene synthones

The synthesis of SF5- and CF3-substituted benzenes and naphthalenes from various 7-oxanorbornene derivatives utilizing SF 5Cl and CF3I radical addition reactions, followed by dehydrohalogenation and aromatizatio

The Diels-Alder Route to Trifluoromethyl-Substituted Carbo- and Heterocycles

Starting with 1,1,1-trifluoroacetone, 3-(trifluoromethyl)-1-(trimethylsilyloxy)-1,3-butadiene (2) has been prepared as a mixture of (Z) and (E) isomers.The diene undergoes cycloaddition reactions with a variety of dienophiles affording trifluoromethyl-substituted carbocyclic and heterocyclic compounds 7-11 in yields ranging from moderate to good. - Keywords: Trifluoromethyl substituents / Carbocycles / Heterocycles / Diels-Alder reactions / Electron-rich/electron-poor diene