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(3-Fluoro-4′-pentyl-[1.1′-biphenyl]-4-yl)boronic acidis a specialized organoboron compound featuring a fluorinated biphenyl framework with a pentyl substituent. This compound is structurally characterized by a fluorine atom at the meta position of one benzene ring and a pentyl chain on the adjacent ring, with the boronic acid group positioned para to the pentyl substituent. Such a configuration endows the molecule with unique electronic properties and steric bulk, influencing its reactivity and applications in organic synthesis and material science.
Свойства ключа
| Объект | Подробнее |
|---|---|
| Название IUPAC | (3-Fluoro-4′-pentyl-[1.1′-biphenyl]-4-yl)boronic acid |
| Номер по CAS | N/A (Specific CAS number may not be available) |
| Молекулярная формула | C₁₇H₂₀BFO₂ (Inferred based on butyl analog) |
| Молекулярная масса | 286.15 g/mol (Calculated based on inferred molecular formula) |
| Внешний вид | White to off-white powder (Inferred based on propyl and butyl analogs) |
| Плотность | N/A (Slightly higher than butyl analog) |
| Точка кипения | N/A (Slightly higher than butyl analog) |
| Показатель преломления | N/A (Similar to propyl and butyl analogs) |
| Точка возгорания | N/A (Similar to propyl and butyl analogs) |
| Метод синтеза | Реакции кросс-сочетания, катализируемые палладием (например, реакция Сузуки-Мияуры) |
| Приложения | Органический синтез, медицинская химия, разработка новых фармацевтических препаратов |
Синтез
The compound is likely synthesized via palladium-catalyzed cross-coupling reactions, such as the Suzuki-Miyaura coupling. This method involves the reaction of a fluorinated aryl halide with a pentyl-substituted arylboronic acid, facilitated by a palladium catalyst, to construct the biphenyl framework efficiently.
Приложения
В органическом синтезе(3-Fluoro-4′-pentyl-[1.1′-biphenyl]-4-yl)boronic acidserves as a valuable building block for the preparation of complex molecules, especially those requiring defined stereochemistry and functionality. The fluorinated biphenyl structure makes it a promising candidate for the development of novel pharmaceuticals, agrochemicals, and functional materials. The boronic acid moiety can be further transformed into other functional groups, expanding the scope of its applications.
Стабильность и хранение
The compound is expected to be stable under normal conditions when stored in a cool, dry place, protected from light and moisture. It is recommended to store it under inert gas to prevent oxidation.
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Фабрика и отгрузка
