AKOS BRN-1038
4-(4-Fluorophenyl)phenylboronic acid
CAS: 140369-67-1
Molecular Formula: C12H10BFO2
AKOS BRN-1038 - Names and Identifiers
| Name | 4-(4-Fluorophenyl)phenylboronic acid |
| Synonyms | AKOS BRN-1038 4'-FLUORO-4-BIPHENYLBORONIC ACID 4'-Fluorobiphenyl-4-boronic acid 4'-fluorobiphenyl-4-ylboronic acid 4-(4-Fluorophenyl)phenylboronic acid (4'-fluoro-[1,1'-biphenyl]-4-yl)boronic acid Boronic acid, B-(4'-fluoro[1,1'-biphenyl]-4-yl)- |
| CAS | 140369-67-1 |
| InChI | InChI=1/C12H10BFO2/c14-12-7-3-10(4-8-12)9-1-5-11(6-2-9)13(15)16/h1-8,15-16H |
AKOS BRN-1038 - Physico-chemical Properties
| Molecular Formula | C12H10BFO2 |
| Molar Mass | 216.02 |
| Density | 1.25±0.1 g/cm3(Predicted) |
| Boling Point | 382.3±44.0 °C(Predicted) |
| Flash Point | 185.014°C |
| Vapor Presure | 0mmHg at 25°C |
| Appearance | Solid |
| pKa | 8.56±0.17(Predicted) |
| Storage Condition | Inert atmosphere,Store in freezer, under -20°C |
| Refractive Index | 1.591 |
AKOS BRN-1038 - Introduction
4-(4-fluorophenyl) phenylboronic acid is an organic compound. It has the molecular formula C12H9BF and the structural formula PhBF2, where Ph represents a phenyl group.
Nature:
4-(4-Fluorophenyl) phenylboronic acid is a colorless crystal, soluble in organic solvents such as ethanol and dimethylformamide. It is relatively stable in air, but decomposes when heated.
Use:
4-(4-Fluorophenyl) phenylboronic acid is mainly used in the field of organic synthesis. It is often used as a ligand for organometallic catalysts to catalyze some important chemical reactions, such as coupling reactions and fluorination reactions. In addition, it can also be used to prepare other organoboron compounds.
Preparation Method:
The common preparation method is to react 4-fluorophenylboronic acid and phenylboronic acid under the catalysis of alkali. The reaction is generally carried out at elevated temperature with dehydration.
Safety Information:
4-(4-fluorophenyl) phenylboronic acid has low toxicity, but as an organic compound, it is still necessary to pay attention to safe operation. Contact with skin, eyes or inhalation of dust may cause irritation and eye irritation. Wear protective gloves and goggles during use and maintain well-ventilated laboratory conditions.
Nature:
4-(4-Fluorophenyl) phenylboronic acid is a colorless crystal, soluble in organic solvents such as ethanol and dimethylformamide. It is relatively stable in air, but decomposes when heated.
Use:
4-(4-Fluorophenyl) phenylboronic acid is mainly used in the field of organic synthesis. It is often used as a ligand for organometallic catalysts to catalyze some important chemical reactions, such as coupling reactions and fluorination reactions. In addition, it can also be used to prepare other organoboron compounds.
Preparation Method:
The common preparation method is to react 4-fluorophenylboronic acid and phenylboronic acid under the catalysis of alkali. The reaction is generally carried out at elevated temperature with dehydration.
Safety Information:
4-(4-fluorophenyl) phenylboronic acid has low toxicity, but as an organic compound, it is still necessary to pay attention to safe operation. Contact with skin, eyes or inhalation of dust may cause irritation and eye irritation. Wear protective gloves and goggles during use and maintain well-ventilated laboratory conditions.
Last Update：2024-04-10 22:29:15
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