4-Bromobenzo[c][1,2,5]oxadiazole
97%
- Product Code: 87005
CAS:
35036-93-2
| Molecular Weight: | 199.00 g./mol | Molecular Formula: | C₆H₃BrN₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18451264 | |
| Melting Point: | 107 °C | Boiling Point: | 255.8±32.0 °C(Predicted) |
| Density: | 1.826±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring a bromine atom attached to a benzooxadiazole ring, makes it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and materials science applications. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce the benzooxadiazole moiety into target molecules. Additionally, its electron-deficient nature makes it useful in the design of organic semiconductors and fluorescent probes for sensing applications. The compound’s reactivity and stability also contribute to its role in the synthesis of heterocyclic compounds with potential biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $208.47 |
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| 0.250 | 10-20 days | $354.29 |
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| 1.000 | 10-20 days | $764.50 |
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4-Bromobenzo[c][1,2,5]oxadiazole
This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring a bromine atom attached to a benzooxadiazole ring, makes it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and materials science applications. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce the benzooxadiazole moiety into target molecules. Additionally, its electron-deficient nature makes it useful in the design of organic semiconductors and fluorescent probes for sensing applications. The compound’s reactivity and stability also contribute to its role in the synthesis of heterocyclic compounds with potential biological activity.
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