850568-04-6
2-Fluoro-5-(methoxycarbonyl)phenylboronic acid
CAS: 850568-04-6
Molecular Formula: C8H8BFO4
850568-04-6 - Names and Identifiers
850568-04-6 - Physico-chemical Properties
| Molecular Formula | C8H8BFO4 |
| Molar Mass | 197.96 |
| Density | 1.33±0.1 g/cm3(Predicted) |
| Melting Point | 210-212 |
| Boling Point | 361.0±52.0 °C(Predicted) |
| Flash Point | 172.123°C |
| Vapor Presure | 0mmHg at 25°C |
| pKa | 7.53±0.58(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
| Refractive Index | 1.514 |
850568-04-6 - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Hazard Note | Irritant |
850568-04-6 - Introduction
2-Fluoro-5-(methoxycarbonyl)phenylboronic acid is an organic compound with the chemical formula C9H8BFNO4 and a molecular weight of 219.97g/mol.
Properties: 2-Fluoro-5-(methoxycarbonyl)phenylboronic acid is a colorless solid with high thermal stability. It is insoluble in water but soluble in organic solvents such as methanol, ethanol and dichloromethane. It is an acid that can react with some bases.
Purpose: 2-Fluoro-5-(methoxycarbonyl)phenylboronic acid is an important organic synthesis intermediate. It is often used in organic synthesis reactions, such as Suzuki coupling reaction, Heck reaction, Sonn-Meviai reaction and so on. It can be used as a raw material for the synthesis of chemical drugs, for the preparation of anti-cancer drugs, pesticides, dyes and functional materials.
Preparation method: The preparation of 2-Fluoro-5-(methoxycarbonyl)phenylboronic acid is usually obtained by reacting 2-fluoro-5-methoxycarbonylbenzeneborate with a boronic acid ligand. The specific preparation method may be a method commonly used in organic synthetic chemistry, such as adding a reactant in an appropriate solvent, and performing the reaction at an appropriate temperature and reaction time.
Safety information: 2-Fluoro-5-(methoxycarbonyl)phenylboronic acid has not been listed on the international or domestic list of dangerous goods. However, it is a chemical, so it should be used and handled in accordance with chemical safety practices. Avoid direct contact with eyes, skin and respiratory tract. Appropriate personal protective equipment, such as lab gloves and goggles, should be worn when used in a laboratory environment.
Properties: 2-Fluoro-5-(methoxycarbonyl)phenylboronic acid is a colorless solid with high thermal stability. It is insoluble in water but soluble in organic solvents such as methanol, ethanol and dichloromethane. It is an acid that can react with some bases.
Purpose: 2-Fluoro-5-(methoxycarbonyl)phenylboronic acid is an important organic synthesis intermediate. It is often used in organic synthesis reactions, such as Suzuki coupling reaction, Heck reaction, Sonn-Meviai reaction and so on. It can be used as a raw material for the synthesis of chemical drugs, for the preparation of anti-cancer drugs, pesticides, dyes and functional materials.
Preparation method: The preparation of 2-Fluoro-5-(methoxycarbonyl)phenylboronic acid is usually obtained by reacting 2-fluoro-5-methoxycarbonylbenzeneborate with a boronic acid ligand. The specific preparation method may be a method commonly used in organic synthetic chemistry, such as adding a reactant in an appropriate solvent, and performing the reaction at an appropriate temperature and reaction time.
Safety information: 2-Fluoro-5-(methoxycarbonyl)phenylboronic acid has not been listed on the international or domestic list of dangerous goods. However, it is a chemical, so it should be used and handled in accordance with chemical safety practices. Avoid direct contact with eyes, skin and respiratory tract. Appropriate personal protective equipment, such as lab gloves and goggles, should be worn when used in a laboratory environment.
Last Update：2024-04-09 20:49:11
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