1486485-43-1

Basic information

• Product Name: 1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-1H-pyrazole, 2-{3-[(1H-Pyrazol-1-yl)methyl]phenyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• Synonyms: 1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-1H-pyrazole, 2-{3-[(1H-Pyrazol-1-yl)methyl]phenyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;3-[(1H-Pyrazol-1-yl)methyl]benzeneboronic acid, pinacol ester
• CAS NO: 1486485-43-1
• Molecular Formula: C16H21BN2O2
• Molecular Weight: 284.16114
• Mol File: 1486485-43-1.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-1H-pyrazole, 2-{3-[(1H-Pyrazol-1-yl)methyl]phenyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-1H-pyrazole, 2-{3-[(1H-Pyrazol-1-yl)methyl]phenyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(1486485-43-1)
• EPA Substance Registry System: 1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]-1H-pyrazole, 2-{3-[(1H-Pyrazol-1-yl)methyl]phenyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(1486485-43-1)

Safety Data

• Hazardous Substances Data: 1486485-43-1(Hazardous Substances Data)

Usage

Chemical structure

The compound contains a pyrazole ring and a boron-containing group (dioxaborolane), with a benzyl group attached to the boron atom.

Functional groups

The compound has a pyrazole ring, a dioxaborolane group, and a benzyl group.

Biological activity

Both pyrazole and dioxaborolane groups have shown biological activity in various studies, suggesting potential applications in medicinal chemistry.

Reactivity

The presence of the benzyl group in the compound may indicate reactivity towards certain organic reactions, making it a potentially useful building block for the synthesis of more complex molecules.

Synthesis

The compound can be synthesized through various organic reactions, such as cross-coupling reactions, which involve the formation of carbon-carbon or carbon-heteroatom bonds.

Stability

The compound is likely to be stable under normal conditions, as both the pyrazole and dioxaborolane groups are known for their stability.

Solubility

The compound may be soluble in organic solvents, such as dimethyl sulfoxide (DMSO) or dimethylformamide (DMF), due to the presence of the benzyl group.

Purity

The purity of the compound can be determined through various analytical techniques, such as high-performance liquid chromatography (HPLC) or mass spectrometry (MS).

Applications

The compound may have potential applications in the development of new drugs, as both the pyrazole and dioxaborolane groups have shown biological activity in various studies.

Safety

As with any chemical compound, proper safety precautions should be taken when handling and storing 1-[3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzyl]-1H-pyrazole, including the use of appropriate personal protective equipment (PPE) and following established laboratory safety protocols.