4-(Benzyloxy)-2-bromo-1-fluorobenzene
97%
- Product Code: 87456
CAS:
1364572-05-3
| Molecular Weight: | 281.12 g./mol | Molecular Formula: | C₁₃H₁₀BrFO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD25320165 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis as an intermediate for the production of more complex molecules. Its structure, featuring bromo and fluoro substituents, makes it a valuable building block in pharmaceutical and agrochemical research. The benzyloxy group provides a protective functionality, allowing selective reactions to occur at other sites of the molecule. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biaryl or aryl-heteroaryl compounds. These reactions are crucial in developing active pharmaceutical ingredients (APIs) or advanced materials. Additionally, its halogenated aromatic ring makes it suitable for further functionalization, enabling the synthesis of diverse chemical entities with potential biological or industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $234.59 |
+
-
|
| 0.250 | 10-20 days | $398.16 |
+
-
|
| 1.000 | 10-20 days | $1,074.44 |
+
-
|
4-(Benzyloxy)-2-bromo-1-fluorobenzene
This chemical is primarily utilized in organic synthesis as an intermediate for the production of more complex molecules. Its structure, featuring bromo and fluoro substituents, makes it a valuable building block in pharmaceutical and agrochemical research. The benzyloxy group provides a protective functionality, allowing selective reactions to occur at other sites of the molecule. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biaryl or aryl-heteroaryl compounds. These reactions are crucial in developing active pharmaceutical ingredients (APIs) or advanced materials. Additionally, its halogenated aromatic ring makes it suitable for further functionalization, enabling the synthesis of diverse chemical entities with potential biological or industrial applications.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
$0.00
$0.00
Total :