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Введение
10- (1-Naphthyl) Anthracene-9-Boronic Acid is a valuable chemical compound with diverse applications in organic synthesis and material science. This compound has the CAS number 400607-46-7. Below is a detailed overview of this compound, presented in a table format for clarity.
| Аспект | Подробнее |
|---|---|
| Номер по CAS | 400607-46-7 |
| Молекулярная формула | C24H17BO2 |
| Молекулярная масса | X |
| Точка кипения | 574.2 ° C при 760 мм рт.ст. |
| Плотность | 1.3 g / cm³ |
| Внешний вид | Твердый порошок |
| Растворимость | Not specified, but should be stored in a sealed, dry, and ventilated area |
| Условия хранения | Store in a cool, ventilated warehouse, temperature should not exceed 37°C, avoid storing with oxidants and food chemicals |
| Приложения | Organic synthesis intermediate, OLED intermediate |
| Информация по технике безопасности | Follow standard chemical safety practices, store in a cool, ventilated area, avoid contact with oxidants and food chemicals |
| Поставщики | Доступно несколько поставщиков, предлагающих различные размеры упаковок и цены. |
химические свойства
10- (1-Naphthyl) Anthracene-9-Boronic Acid has a molecular formula of C24H17BO2 and a molecular weight of 348.20 g/mol. Its boiling point is 574.2°C at 760 mmHg, and its density is 1.3 g/cm³. The compound appears as a solid powder. While specific solubility information is not provided, it is recommended to store the compound in a sealed, dry, and ventilated area. The storage conditions should be in a cool, ventilated warehouse where the temperature does not exceed 37°C, and it should be kept away from oxidants and food chemicals.
Приложения
This compound is primarily used as an organic synthesis intermediate, particularly in the synthesis of conjugated organic materials. It has the potential to be used in Suzuki coupling reactions to introduce specific groups, thereby altering the luminescence and structural properties of the materials. Additionally, it serves as an intermediate in the production of Organic Light-Emitting Diodes (OLEDs).
Синтез
The conventional synthesis of 10- (1-Naphthyl) Anthracene-9-Boronic Acid involves starting with 9-bromo-10-(1-naphthyl)anthracene. Under strong basic conditions, the bromine atom on the anthracene ring is removed to generate an aryl lithium reagent. This reagent is then reacted with trimethyl borate or triisopropyl borate, followed by hydrolysis to yield the boronic acid compound. However, specific synthesis steps and conditions are not detailed.
Информация по технике безопасности
While specific hazard information is not provided, it is recommended to follow standard chemical safety practices when handling 10- (1-Naphthyl) Anthracene-9-Boronic Acid. This includes storing the compound in a cool, ventilated area and avoiding contact with oxidants and food chemicals.
Поставщики
Several suppliers offer 10- (1-Naphthyl) Anthracene-9-Boronic Acid in various package sizes and at different prices. For instance, some suppliers offer 250 milligrams for approximately 51.90 yuan and 1 gram for about 469.90 yuan. This allows researchers and manufacturers to purchase the quantity that best suits their needs.
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Фабрика и отгрузка
