1308298-23-8

Basic information

• Product Name: 2-(trifluoroMethyl)pyriMidin-5-ylboronic acid
• Synonyms: 2-(trifluoroMethyl)pyriMidin-5-ylboronic acid;[2-(Trifluoromethyl)-5-pyrimidinyl]boronic acid;4-Trifluormethyl-phenothiazin
• CAS NO: 1308298-23-8
• Molecular Formula: C₅H₄BF₃N₂O₂
• Molecular Weight: 191.9036696
• Mol File: 1308298-23-8.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 236.7±50.0 °C(Predicted)
• Appearance: /
• Density: 1.53±0.1 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 4.46±0.11(Predicted)
• CAS DataBase Reference: 2-(trifluoroMethyl)pyriMidin-5-ylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(trifluoroMethyl)pyriMidin-5-ylboronic acid(1308298-23-8)
• EPA Substance Registry System: 2-(trifluoroMethyl)pyriMidin-5-ylboronic acid(1308298-23-8)

Safety Data

• Hazardous Substances Data: 1308298-23-8(Hazardous Substances Data)

Usage

General Description

2-(trifluoroMethyl)pyriMidin-5-ylboronic acid is a chemical compound with the molecular formula C6H5BF3N3O2. It is a boronic acid derivative that contains a trifluoromethyl group and a pyrimidine ring. 2-(trifluoroMethyl)pyriMidin-5-ylboronic acid is commonly used in organic synthesis and medicinal chemistry as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its boronic acid functionality makes it useful for Suzuki-Miyaura cross-coupling reactions, which are widely employed in the synthesis of biologically active molecules. The trifluoromethyl group also imparts unique physicochemical properties to the compound, making it a valuable tool in drug discovery and development. Furthermore, the pyrimidine ring provides opportunities for potential interactions with biological targets, making 2-(trifluoroMethyl)pyriMidin-5-ylboronic acid a versatile and important chemical in the field of medicinal chemistry.