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Номер CAS: 1030825-20-7Внешний вид: белый порошокМолекулярная формула: C18H14BrFSЧистота: ВЭЖХ≥99.5%М...
Номер CAS: 1030825-20-7
Внешний вид: белый порошок
Молекулярная формула: C18H14BrFS
Чистота: ВЭЖХ≥99.5%
Мощность:20 тонн/месяц
Молекулярная масса: 361.27
Применение: промежуточные продукты каглифлозина, фармацевтические промежуточные продукты
Объект | Подробнее |
---|---|
Молекулярная формула | C18H14BrFS |
Молекулярная масса | X |
Внешний вид | Off-white to pale yellow crystalline solid or powder |
чистота | Обычно ≥95% (ВЭЖХ) |
Температура плавления | Data not widely available; likely in the range of 150-200 °C |
Точка кипения | Predicted to be high; exact data not available |
Плотность | Approximately 1.4-1.5 g/cm³ (Predicted based on structure) |
Точка возгорания | Predicted to be above 200 °C |
Растворимость | Soluble in organic solvents such as DMSO, chloroform, and toluene |
Приложения | Organic synthesis, pharmaceutical research, materials science |
Метод синтеза | Typically involves coupling reactions and functional group manipulations |
Вопросы безопасности | Обращаться осторожно; избегать контакта с кожей и глазами; использовать в хорошо проветриваемом помещении. |
Память | Хранить в сухом, прохладном месте, защищенном от света и влаги. |
Поставщики | Available through custom synthesis from specialized chemical suppliers |
2-(2-Methyl-5-bromobenzyl)-5-(4-fluorophenyl)thiophene is a complex organic compound with a molecular formula of C18H14BrFS and a molecular weight of 361.27 g/mol. It typically appears as an off-white to pale yellow crystalline solid or powder with a purity of ≥95% as determined by HPLC. The melting point of this compound is not widely available but is likely in the range of 150-200 °C. It is soluble in organic solvents such as DMSO, chloroform, and toluene, making it suitable for various chemical reactions and syntheses.
This compound finds applications in organic synthesis, particularly in the development of new pharmaceutical compounds and materials. Its unique structure, featuring a thiophene ring substituted with a bromobenzyl and a fluorophenyl group, provides a versatile platform for further chemical modifications.
The synthesis of 2-(2-Methyl-5-bromobenzyl)-5-(4-fluorophenyl)thiophene typically involves coupling reactions and functional group manipulations, requiring careful control of reaction conditions. When handling this compound, appropriate safety measures should be taken, including the use of protective equipment and working in a well-ventilated area.
This compound may not be readily available off-the-shelf and may require custom synthesis from specialized chemical suppliers. Researchers interested in this compound should consult with suppliers to obtain detailed synthesis protocols and safety data sheets.