1-Bromo-5-chloro-2,3-difluorobenzene
98%
- Product Code: 40048
CAS:
1160573-26-1
Molecular Weight: | 227.43 g./mol | Molecular Formula: | C₆H₂BrClF₂ |
---|---|---|---|
EC Number: | MDL Number: | MFCD11845996 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
1-Bromo-5-chloro-2,3-difluorobenzene is primarily utilized as a versatile intermediate in organic synthesis. Its unique combination of halogen substituents makes it valuable for constructing complex molecules, particularly in pharmaceutical and agrochemical research. The compound is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic structures with specific halogen patterns. These reactions are crucial for developing active pharmaceutical ingredients (APIs) or advanced materials. Additionally, its halogen-rich structure allows for further functionalization, enabling the creation of diverse chemical entities for drug discovery or specialty chemical applications. The presence of fluorine atoms also enhances the metabolic stability and bioavailability of resulting compounds, making it a preferred choice in medicinal chemistry.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
---|---|---|---|
1.000 | 10-20 days | ฿4,482.00 |
+
-
|
5.000 | 10-20 days | ฿20,592.00 |
+
-
|
1-Bromo-5-chloro-2,3-difluorobenzene
1-Bromo-5-chloro-2,3-difluorobenzene is primarily utilized as a versatile intermediate in organic synthesis. Its unique combination of halogen substituents makes it valuable for constructing complex molecules, particularly in pharmaceutical and agrochemical research. The compound is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic structures with specific halogen patterns. These reactions are crucial for developing active pharmaceutical ingredients (APIs) or advanced materials. Additionally, its halogen-rich structure allows for further functionalization, enabling the creation of diverse chemical entities for drug discovery or specialty chemical applications. The presence of fluorine atoms also enhances the metabolic stability and bioavailability of resulting compounds, making it a preferred choice in medicinal chemistry.
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 :