475250-46-5

Basic information

• Product Name: 4-(Trifluoromethyl)benzylboronic acid pinacol ester
• Synonyms: 4-(trifluoromethyl)benzylboronic acid pinacol ester;2-(4-(Trifluoromethyl)benzyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;4,4,5,5-TetraMethyl-2-(4-(trifluoroMethyl)benzyl)-1,3,2-dioxaborolane;3-hydroxy-2,3-dimethylbutan-2-yl hydrogen 4-(trifluoromethyl)benzylboronate;4-(Trifluoromethyl)benzylboronic acid picol ester;4,4,5,5-tetramethyl-2-[[4-(trifluoromethyl)phenyl]methyl]-1,3,2-dioxaborolane
• CAS NO: 475250-46-5
• Molecular Formula: C14H20BF3O3
• Molecular Weight: 286.1
• Mol File: 475250-46-5.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 285 °C
• Flash Point: 126 °C
• Appearance: /
• Density: 1.13
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 4-(Trifluoromethyl)benzylboronic acid pinacol ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(Trifluoromethyl)benzylboronic acid pinacol ester(475250-46-5)
• EPA Substance Registry System: 4-(Trifluoromethyl)benzylboronic acid pinacol ester(475250-46-5)

Safety Data

• Hazardous Substances Data: 475250-46-5(Hazardous Substances Data)

Usage

General Description

4-(Trifluoromethyl)benzylboronic acid pinacol ester is a chemical compound that is commonly used in organic synthesis as a boronic acid derivative. It has a trifluoromethyl group attached to a benzene ring, making it valuable for use in pharmaceutical and agrochemical research due to its strong electron-withdrawing properties. The pinacol ester moiety provides stability and enhances the reactivity of the boronic acid group, allowing for efficient cross-coupling reactions with various organic substrates. 4-(Trifluoromethyl)benzylboronic acid pinacol ester's versatility and reactivity make it a valuable building block in the production of complex organic molecules and potential drug candidates.