4-Bromo-1,2-bis(trifluoromethyl)benzene

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Reagent Code: #117239
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CAS Number 320-29-6

science Other reagents with same CAS 320-29-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.00 g/mol
Formula C₈H₃BrF₆
badge Registry Numbers
MDL Number MFCD06253758
thermostat Physical Properties
Boiling Point 181.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description 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.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,674.00
inventory 1g
10-20 days ฿3,348.00

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4-Bromo-1,2-bis(trifluoromethyl)benzene
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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 trifluorometh

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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