2-Chloro-1-(3,4-difluoro-phenyl)-ethanone
>95%
- Product Code: 42809
CAS:
51336-95-9
| Molecular Weight: | 190.57 g./mol | Molecular Formula: | C₈H₅ClF₂O |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃, dry, away from light |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring a chloroethyl group and difluorophenyl moiety, makes it a versatile building block for constructing more complex molecules. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) that target specific biological pathways, particularly in the development of drugs with anti-inflammatory, antimicrobial, or anticancer properties. Additionally, its reactivity allows for further functionalization, enabling the creation of compounds with tailored properties for specific applications in medicinal chemistry. In agrochemical research, it serves as a precursor for developing herbicides or fungicides, leveraging its ability to interact with biological systems effectively.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 95 100% |
| Appearance | White to light yellow crystal or block |
| INFRARED SPECTRUM | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $63.79 |
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| 25.000 | 10-20 days | $201.91 |
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2-Chloro-1-(3,4-difluoro-phenyl)-ethanone
This compound is primarily utilized in organic synthesis as a key intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring a chloroethyl group and difluorophenyl moiety, makes it a versatile building block for constructing more complex molecules. It is often employed in the synthesis of active pharmaceutical ingredients (APIs) that target specific biological pathways, particularly in the development of drugs with anti-inflammatory, antimicrobial, or anticancer properties. Additionally, its reactivity allows for further functionalization, enabling the creation of compounds with tailored properties for specific applications in medicinal chemistry. In agrochemical research, it serves as a precursor for developing herbicides or fungicides, leveraging its ability to interact with biological systems effectively.
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