1-Bromo-3-chloro-5-(difluoromethoxy)benzene

95%

Reagent Code: #40026
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CAS Number 1004112-67-7

science Other reagents with same CAS 1004112-67-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.4599 g/mol
Formula C₇H₄BrClF₂O
badge Registry Numbers
MDL Number MFCD18390894
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the development of more complex molecules. Its structure, featuring bromo and chloro substituents, makes it a valuable intermediate in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for constructing pharmaceuticals, agrochemicals, and advanced materials. The difluoromethoxy group enhances its utility by providing unique electronic properties, often improving the bioavailability or stability of the final compounds. Additionally, it is employed in the synthesis of liquid crystals and other functional materials due to its ability to influence molecular alignment and phase behavior. Its applications are particularly significant in medicinal chemistry, where it contributes to the creation of drug candidates targeting various diseases.

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inventory 250mg
10-20 days ฿2,484.00

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1-Bromo-3-chloro-5-(difluoromethoxy)benzene
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This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the development of more complex molecules. Its structure, featuring bromo and chloro substituents, makes it a valuable intermediate in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for constructing pharmaceuticals, agrochemicals, and advanced materials. The difluoromethoxy group enhances its utility by providing unique electronic properties

This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the development of more complex molecules. Its structure, featuring bromo and chloro substituents, makes it a valuable intermediate in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential for constructing pharmaceuticals, agrochemicals, and advanced materials. The difluoromethoxy group enhances its utility by providing unique electronic properties, often improving the bioavailability or stability of the final compounds. Additionally, it is employed in the synthesis of liquid crystals and other functional materials due to its ability to influence molecular alignment and phase behavior. Its applications are particularly significant in medicinal chemistry, where it contributes to the creation of drug candidates targeting various diseases.

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