4-Bromo-1,2-bis(trifluoromethyl)benzene
97%
- Product Code: 117239
CAS:
320-29-6
| Molecular Weight: | 293.00 g./mol | Molecular Formula: | C₈H₃BrF₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06253758 | |
| Melting Point: | Boiling Point: | 181.6°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
4-Bromo-1,2-bis(trifluoromethyl)benzene is primarily used in organic synthesis as a versatile building block for the development of more complex chemical compounds. Its structure, featuring both bromine and trifluoromethyl groups, makes it particularly valuable in the creation of pharmaceuticals, agrochemicals, and specialty materials. The bromine atom serves as a reactive site for cross-coupling reactions, such as Suzuki or Heck couplings, enabling the formation of carbon-carbon bonds. The trifluoromethyl groups enhance the stability and lipophilicity of the resulting compounds, which is beneficial in drug design for improving bioavailability and metabolic resistance. Additionally, this compound is employed in the synthesis of liquid crystals and advanced polymers, where its unique electronic properties contribute to desired material characteristics. Its applications also extend to the field of organic electronics, where it aids in the development of components for devices like OLEDs and semiconductors.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,674.00 |
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| 1.000 | 10-20 days | ฿3,348.00 |
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4-Bromo-1,2-bis(trifluoromethyl)benzene
4-Bromo-1,2-bis(trifluoromethyl)benzene is primarily used in organic synthesis as a versatile building block for the development of more complex chemical compounds. Its structure, featuring both bromine and trifluoromethyl groups, makes it particularly valuable in the creation of pharmaceuticals, agrochemicals, and specialty materials. The bromine atom serves as a reactive site for cross-coupling reactions, such as Suzuki or Heck couplings, enabling the formation of carbon-carbon bonds. The trifluoromethyl groups enhance the stability and lipophilicity of the resulting compounds, which is beneficial in drug design for improving bioavailability and metabolic resistance. Additionally, this compound is employed in the synthesis of liquid crystals and advanced polymers, where its unique electronic properties contribute to desired material characteristics. Its applications also extend to the field of organic electronics, where it aids in the development of components for devices like OLEDs and semiconductors.
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