2-FLUORO-4-BIPHENYLBORONIC ACID - Names and Identifiers
2-FLUORO-4-BIPHENYLBORONIC ACID - Physico-chemical Properties
Molecular Formula | C12H10BFO2
|
Molar Mass | 216.02 |
Density | 1.25±0.1 g/cm3(Predicted) |
Melting Point | 243-248 °C (lit.) |
Boling Point | 377.3±52.0 °C(Predicted) |
Flash Point | 186.131°C |
Vapor Presure | 0mmHg at 25°C |
pKa | 7.52±0.10(Predicted) |
Storage Condition | Room Temprature |
Refractive Index | 1.591 |
MDL | MFCD01075707 |
2-FLUORO-4-BIPHENYLBORONIC ACID - Risk and Safety
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin.
R34 - Causes burns
|
Safety Description | S22 - Do not breathe dust.
S24/25 - Avoid contact with skin and eyes.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S27 - Take off immediately all contaminated clothing.
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S37 - Wear suitable gloves.
|
WGK Germany | 3 |
HS Code | 29319090 |
Hazard Note | Irritant/Keep Cold |
Hazard Class | IRRITANT |
2-FLUORO-4-BIPHENYLBORONIC ACID - Introduction
acid is an organic boron compound with the chemical formula C12H9BF, which has the following properties:
1. Appearance: It is colorless crystal or white crystalline powder.
2. Melting point: Its melting point is about 180-183 degrees Celsius.
3. Solubility: It has good solubility in some organic solvents (such as benzene and ethanol), but its solubility in water is low.
acid has a number of important uses in chemical research and industry, including:
1. Catalyst: It can be used as a catalyst for organic synthesis reactions, such as halogenation reactions, carbon-nitrogen coupling reactions, etc.
2. Fluorescent probe: Because of its fluorescence properties, it can be used as a fluorescent probe in fluorescence microscopy and biological imaging.
3. Hybrid materials: It can be combined with other materials to construct inorganic-organic hybrid materials, providing a new application approach for optoelectronic devices.
The method of preparing the Ti-acid mainly includes the following steps:
1. The reaction is first carried out by reacting phenyl magnesium bromide with methyl borate to obtain phenyl boronic acid.
br>2. Then the Phenylboronic acid is fluorinated with fluorine and copper catalyst in an organic solvent to obtain the final acid product.
when using and operating acid, you need to pay attention to the following safety information:
1. Because of its flammable organic solvent, avoid contact with open flame and avoid inhalation of its vapor.
2. In case of contact with skin and eyes, immediately rinse with water for at least 15 minutes and seek medical treatment.
3. Avoid prolonged or frequent contact and use personal protective equipment such as protective gloves and safety glasses.
4. When storing, it should be kept in a dry, cool, well-ventilated place, away from open flames and oxidants.
Please note that acid is a chemical and must be used reasonably under suitable laboratory conditions and follow relevant safety procedures.
Last Update:2024-04-10 22:29:15