Methyl 3-bromo-4-chloro-5-fluorobenzoate
≥95%
- Product Code: 117995
CAS:
1160574-62-8
| Molecular Weight: | 267.48 g./mol | Molecular Formula: | C₈H₅BrClFO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11846086 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in organic synthesis as an intermediate for the development of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for the creation of active pharmaceutical ingredients (APIs). The presence of multiple halogen substituents makes it a versatile precursor for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, which are essential in drug discovery and development. Additionally, it can be utilized in material science for the synthesis of specialized polymers or coatings that require specific halogenated aromatic compounds. Its role in agrochemical research is also notable, as it contributes to the development of novel pesticides or herbicides with targeted activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,728.00 |
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| 5.000 | 10-20 days | ฿5,175.00 |
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| 25.000 | 10-20 days | ฿20,097.00 |
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Methyl 3-bromo-4-chloro-5-fluorobenzoate
This chemical is primarily used in organic synthesis as an intermediate for the development of more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for the creation of active pharmaceutical ingredients (APIs). The presence of multiple halogen substituents makes it a versatile precursor for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, which are essential in drug discovery and development. Additionally, it can be utilized in material science for the synthesis of specialized polymers or coatings that require specific halogenated aromatic compounds. Its role in agrochemical research is also notable, as it contributes to the development of novel pesticides or herbicides with targeted activity.
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