1202054-12-3

Basic information

• Product Name: 5-TRIFLUOROMETHYL-1H-PYRAZOL-4-YLBORONIC ACID
• Synonyms: 5-TRIFLUOROMETHYL-1H-PYRAZOL-4-YLBORONIC ACID;Boronic acid, B-[3-(trifluoroMethyl)-1H-pyrazol-4-yl]-
• CAS NO: 1202054-12-3
• Molecular Formula: C4H4BF3N2O2
• Molecular Weight: 179.8929696
• Mol File: 1202054-12-3.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 388.4±52.0 °C(Predicted)
• Appearance: /
• Density: 1.60±0.1 g/cm3(Predicted)
• Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
• PKA: 7.25±0.58(Predicted)
• CAS DataBase Reference: 5-TRIFLUOROMETHYL-1H-PYRAZOL-4-YLBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 5-TRIFLUOROMETHYL-1H-PYRAZOL-4-YLBORONIC ACID(1202054-12-3)
• EPA Substance Registry System: 5-TRIFLUOROMETHYL-1H-PYRAZOL-4-YLBORONIC ACID(1202054-12-3)

Safety Data

• Hazardous Substances Data: 1202054-12-3(Hazardous Substances Data)

Usage

General Description

5-Trifluoromethyl-1H-pyrazol-4-ylboronic acid is a boronic acid derivative that contains a pyrazole ring with a trifluoromethyl substituent at the 5th position. It is commonly used as a reagent in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. The boronic acid moiety allows it to participate in Suzuki-Miyaura cross-coupling reactions and other transition metal-catalyzed processes. The trifluoromethyl group enhances the reactivity and selectivity of the compound in various transformations. This chemical has found applications in medicinal chemistry, agrochemical synthesis, and material science due to its versatile nature and ability to functionalize complex molecules.