1-Bromo-3-chloro-5-(difluoromethoxy)benzene
95%
- Product Code: 40026
CAS:
1004112-67-7
Molecular Weight: | 257.4599 g./mol | Molecular Formula: | C₇H₄BrClF₂O |
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EC Number: | MDL Number: | MFCD18390894 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
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.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿2,484.00 |
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1-Bromo-3-chloro-5-(difluoromethoxy)benzene
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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