2-Bromo-4-Iodo-1-(Trifluoromethoxy)Benzene
≥98%
- Product Code: 78189
CAS:
1049731-04-5
| Molecular Weight: | 366.9 g./mol | Molecular Formula: | C₇H₃BrF₃IO |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex molecules. Its unique structure, featuring both bromine and iodine substituents, makes it a valuable building block in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in pharmaceutical and agrochemical research. The trifluoromethoxy group enhances its utility in the design of compounds with improved metabolic stability and bioavailability, often sought after in drug discovery. Additionally, it serves as a precursor in the synthesis of liquid crystals and advanced materials, where its halogenated aromatic core contributes to desired electronic and optical properties. Its applications are particularly prominent in the development of active pharmaceutical ingredients (APIs) and specialty chemicals.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | €75.98 |
+
-
|
| 1.000 | 10-20 days | €197.07 |
+
-
|
2-Bromo-4-Iodo-1-(Trifluoromethoxy)Benzene
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex molecules. Its unique structure, featuring both bromine and iodine substituents, makes it a valuable building block in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in pharmaceutical and agrochemical research. The trifluoromethoxy group enhances its utility in the design of compounds with improved metabolic stability and bioavailability, often sought after in drug discovery. Additionally, it serves as a precursor in the synthesis of liquid crystals and advanced materials, where its halogenated aromatic core contributes to desired electronic and optical properties. Its applications are particularly prominent in the development of active pharmaceutical ingredients (APIs) and specialty chemicals.
| 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 :