(3-fluoro-2-formylphenyl)boronic acid
(3-fluoro-2-formylphenyl)boronic acid
CAS: 871126-15-7
Molecular Formula: C7H6BFO3
(3-fluoro-2-formylphenyl)boronic acid - Names and Identifiers
(3-fluoro-2-formylphenyl)boronic acid - Physico-chemical Properties
| Molecular Formula | C7H6BFO3 |
| Molar Mass | 167.93 |
| Density | 1.33±0.1 g/cm3(Predicted) |
| Melting Point | 123-127℃ |
| Boling Point | 357.4±52.0 °C(Predicted) |
| Water Solubility | Slightly soluble in water. |
| Appearance | Solid |
| pKa | 7.15±0.53(Predicted) |
| Storage Condition | 2-8°C |
| Sensitive | Light Sensitive |
(3-fluoro-2-formylphenyl)boronic acid - Risk and Safety
| Hazard Symbols | C - Corrosive |
| Risk Codes | 34 - Causes burns |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
| UN IDs | UN 3261 8/PG 2 |
| WGK Germany | 3 |
| Hazard Class | 8 |
| Packing Group | Ⅱ |
(3-fluoro-2-formylphenyl)boronic acid - Introduction
(3-fluoro-2-formylphenyl)boronic acid is an organic compound with the chemical formula C7H6BFO3.
Nature:
-Appearance: colorless crystalline powder
-Melting point: about 120-121°C
-Solubility: Soluble in organic solvents such as dimethyl sulfoxide and dichloromethane, slightly soluble in ethanol and chloroform
Use:
(3-fluoro-2-formylphenyl)boronic acid is a commonly used reagent in organic synthesis, used to synthesize organic compounds containing aromatic aldehyde groups. It can be used as the starting material of aromatic aldehyde groups in organic synthesis, and participate in the aldehyde reaction, aryl boronic acid reaction and so on. In addition, it has applications in the field of drug synthesis and medicine.
Preparation Method:
(3-fluoro-2-formylphenyl)boronic acid is often synthesized by aromatic boration. The specific method is to react 3-fluoro-2-nitrobenzene boronic acid and diethyl borate under mild conditions to generate (3-fluoro-2-formylphenyl)boronic acid. The reaction process requires the use of suitable solvents and catalysts, and appropriate temperature and time control.
Safety Information:
(3-fluoro-2-formylphenyl) There is no specific safety risk report for boronic acid, but as an organic compound, it is still necessary to pay attention to safety when using it. Avoid contact with skin and eyes, avoid inhalation or ingestion. Wear appropriate protective equipment, such as gloves, goggles and protective clothing. During use and storage, avoid contact with oxidants and combustibles to prevent fire or smoke.
Nature:
-Appearance: colorless crystalline powder
-Melting point: about 120-121°C
-Solubility: Soluble in organic solvents such as dimethyl sulfoxide and dichloromethane, slightly soluble in ethanol and chloroform
Use:
(3-fluoro-2-formylphenyl)boronic acid is a commonly used reagent in organic synthesis, used to synthesize organic compounds containing aromatic aldehyde groups. It can be used as the starting material of aromatic aldehyde groups in organic synthesis, and participate in the aldehyde reaction, aryl boronic acid reaction and so on. In addition, it has applications in the field of drug synthesis and medicine.
Preparation Method:
(3-fluoro-2-formylphenyl)boronic acid is often synthesized by aromatic boration. The specific method is to react 3-fluoro-2-nitrobenzene boronic acid and diethyl borate under mild conditions to generate (3-fluoro-2-formylphenyl)boronic acid. The reaction process requires the use of suitable solvents and catalysts, and appropriate temperature and time control.
Safety Information:
(3-fluoro-2-formylphenyl) There is no specific safety risk report for boronic acid, but as an organic compound, it is still necessary to pay attention to safety when using it. Avoid contact with skin and eyes, avoid inhalation or ingestion. Wear appropriate protective equipment, such as gloves, goggles and protective clothing. During use and storage, avoid contact with oxidants and combustibles to prevent fire or smoke.
Last Update：2024-04-09 02:00:48
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CAS: 871126-15-7
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