(2-Bromo-5-fluorophenoxy)acetonitrile
≥95%
- Product Code: 80703
CAS:
874804-05-4
| Molecular Weight: | 230.03 g./mol | Molecular Formula: | C₈H₅BrFNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06409081 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily utilized in organic synthesis as a building block for the development of more complex molecules. It is often employed in the pharmaceutical industry to create intermediates that are further processed into active pharmaceutical ingredients (APIs). Its specific structure, featuring both bromine and fluorine substituents, makes it valuable for introducing halogenated aromatic moieties into target compounds, which can enhance biological activity or alter pharmacokinetic properties. Additionally, it is used in agrochemical research to develop novel pesticides or herbicides, where the halogen atoms play a crucial role in the compound's efficacy. Its reactivity as a nitrile also allows it to participate in various chemical transformations, such as cyclization or coupling reactions, making it a versatile reagent in synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,850.00 |
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(2-Bromo-5-fluorophenoxy)acetonitrile
This chemical is primarily utilized in organic synthesis as a building block for the development of more complex molecules. It is often employed in the pharmaceutical industry to create intermediates that are further processed into active pharmaceutical ingredients (APIs). Its specific structure, featuring both bromine and fluorine substituents, makes it valuable for introducing halogenated aromatic moieties into target compounds, which can enhance biological activity or alter pharmacokinetic properties. Additionally, it is used in agrochemical research to develop novel pesticides or herbicides, where the halogen atoms play a crucial role in the compound's efficacy. Its reactivity as a nitrile also allows it to participate in various chemical transformations, such as cyclization or coupling reactions, making it a versatile reagent in synthetic chemistry.
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