3-Bromo-5-phenyl-1,2,4-oxadiazole
95%
- Product Code: 45301
CAS:
23432-94-2
Molecular Weight: | 225.0500 g./mol | Molecular Formula: | C₈H₅BrN₂O |
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EC Number: | MDL Number: | MFCD06795878 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex chemical structures. Its unique structure, featuring both a bromine atom and an oxadiazole ring, makes it a valuable intermediate in the preparation of pharmaceuticals and agrochemicals. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce phenyl or other aromatic groups into target molecules. Additionally, its oxadiazole core is of interest in the design of bioactive compounds, particularly in the development of potential drugs with antimicrobial, anti-inflammatory, or anticancer properties. Researchers also explore its use in material science for the synthesis of organic electronic materials due to its electron-deficient nature.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $125.96 |
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3-Bromo-5-phenyl-1,2,4-oxadiazole
This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex chemical structures. Its unique structure, featuring both a bromine atom and an oxadiazole ring, makes it a valuable intermediate in the preparation of pharmaceuticals and agrochemicals. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce phenyl or other aromatic groups into target molecules. Additionally, its oxadiazole core is of interest in the design of bioactive compounds, particularly in the development of potential drugs with antimicrobial, anti-inflammatory, or anticancer properties. Researchers also explore its use in material science for the synthesis of organic electronic materials due to its electron-deficient nature.
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