2,4-Dibromo-1,3,5-trifluorobenzene
97%
- Product Code: 115338
CAS:
363-69-9
Molecular Weight: | 289.88 g./mol | Molecular Formula: | C₆HBr₂F₃ |
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EC Number: | MDL Number: | MFCD11845962 | |
Melting Point: | Boiling Point: | 8590°C at 20 mmHg | |
Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
2,4-Dibromo-1,3,5-trifluorobenzene is primarily used as an intermediate in organic synthesis, particularly in the production of complex chemical compounds. Its structure, featuring both bromine and fluorine atoms, makes it valuable in the development of pharmaceuticals, agrochemicals, and specialty chemicals. The compound is often utilized in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create more complex molecules with specific properties. Additionally, it serves as a building block in the synthesis of materials for electronic applications, including organic semiconductors and liquid crystals, due to its ability to modify electronic properties and enhance stability. Its halogenated nature also makes it suitable for use in flame retardants and other industrial applications where halogenated compounds are required.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿279.00 |
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0.250 | 10-20 days | ฿387.00 |
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1.000 | 10-20 days | ฿1,098.00 |
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5.000 | 10-20 days | ฿4,509.00 |
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2,4-Dibromo-1,3,5-trifluorobenzene
2,4-Dibromo-1,3,5-trifluorobenzene is primarily used as an intermediate in organic synthesis, particularly in the production of complex chemical compounds. Its structure, featuring both bromine and fluorine atoms, makes it valuable in the development of pharmaceuticals, agrochemicals, and specialty chemicals. The compound is often utilized in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create more complex molecules with specific properties. Additionally, it serves as a building block in the synthesis of materials for electronic applications, including organic semiconductors and liquid crystals, due to its ability to modify electronic properties and enhance stability. Its halogenated nature also makes it suitable for use in flame retardants and other industrial applications where halogenated compounds are required.
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