(3-(萘-1-基)苯基)硼酸
3-(1-Naphthyl)phenylboronic acid
CAS: 881913-20-8
Molecular Formula: C16H13BO2
(3-(萘-1-基)苯基)硼酸 - Names and Identifiers
(3-(萘-1-基)苯基)硼酸 - Physico-chemical Properties
| Molecular Formula | C16H13BO2 |
| Molar Mass | 248.08 |
| Density | 1.23±0.1 g/cm3(Predicted) |
| Boling Point | 471.9±48.0 °C(Predicted) |
| Appearance | Powder |
| Color | Off-white |
| pKa | 8.27±0.19(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
(3-(萘-1-基)苯基)硼酸 - Introduction
3-(1-Naphthyl)phenylboronic acid is an organic compound with the chemical formula C16H13BO2. Its properties are as follows:
1. Appearance: 3-(1-Naphthyl)phenylboronic acid is a white crystalline solid.
2. Solubility: Its solubility in water is low, but it can be dissolved in some organic solvents, such as ethanol and dimethylformamide.
3. Stability: 3-(1-Naphthyl)phenylboronic acid is relatively stable, but oxidation reaction may occur in the presence of strong oxidant.
3-(1-Naphthyl)phenylboronic acid has many uses in organic synthesis:
1. Ligand: It can be used as a ligand to participate in metal-catalyzed reactions, such as organic synthesis reactions catalyzed by copper oxide.
2. precursor of transition metal complex: it can react with transition metal to generate transition metal complex, which can be used in catalysis, photoelectric materials and other fields.
3. Reagent in organic synthesis: 3-(1-Naphthyl)phenylboronic acid can be used as a reagent in organic synthesis, such as the synthesis of aryl borate.
The method for preparing 3-(1-Naphthyl)phenylboronic acid is usually a coupling reaction between 1-naphthylboronic acid and benzoic acid. The specific preparation method can refer to the relevant organic synthesis literature or patent.
For safety information, 3-(1-Naphthyl)phenylboronic acid should be stored in a dry, cool place, away from fire and oxidizing agents. Appropriate personal protective equipment such as laboratory gloves and eye protection should be worn during operation. In addition, relevant laboratory safety regulations and operating guidelines should be followed. If necessary, refer to the Safety Data Sheet (SDS) for detailed safety information.
1. Appearance: 3-(1-Naphthyl)phenylboronic acid is a white crystalline solid.
2. Solubility: Its solubility in water is low, but it can be dissolved in some organic solvents, such as ethanol and dimethylformamide.
3. Stability: 3-(1-Naphthyl)phenylboronic acid is relatively stable, but oxidation reaction may occur in the presence of strong oxidant.
3-(1-Naphthyl)phenylboronic acid has many uses in organic synthesis:
1. Ligand: It can be used as a ligand to participate in metal-catalyzed reactions, such as organic synthesis reactions catalyzed by copper oxide.
2. precursor of transition metal complex: it can react with transition metal to generate transition metal complex, which can be used in catalysis, photoelectric materials and other fields.
3. Reagent in organic synthesis: 3-(1-Naphthyl)phenylboronic acid can be used as a reagent in organic synthesis, such as the synthesis of aryl borate.
The method for preparing 3-(1-Naphthyl)phenylboronic acid is usually a coupling reaction between 1-naphthylboronic acid and benzoic acid. The specific preparation method can refer to the relevant organic synthesis literature or patent.
For safety information, 3-(1-Naphthyl)phenylboronic acid should be stored in a dry, cool place, away from fire and oxidizing agents. Appropriate personal protective equipment such as laboratory gloves and eye protection should be worn during operation. In addition, relevant laboratory safety regulations and operating guidelines should be followed. If necessary, refer to the Safety Data Sheet (SDS) for detailed safety information.
Last Update：2024-04-10 22:29:15
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