5,6-Difluoro-o-anisaldehyde
97%
- Product Code: 174552
CAS:
187543-87-9
| Molecular Weight: | 172.13 g./mol | Molecular Formula: | C₈H₆F₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02093968 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, stored in inert gas |
Product Description:
Used in the synthesis of fluorinated organic compounds, particularly in pharmaceuticals and agrochemicals where fluorine substitution enhances metabolic stability and bioavailability. Serves as a building block in the preparation of active pharmaceutical ingredients (APIs) requiring difluorinated aromatic aldehydes. Its aldehyde and methoxy functional groups allow for versatile reactivity, including condensation and nucleophilic addition reactions. Commonly employed in the development of fluorinated analogs of biologically active molecules, such as kinase inhibitors or anti-inflammatory agents. Also utilized in materials science for constructing fluorinated liquid crystals or organic electronic materials due to the electron-withdrawing effect of fluorine atoms and the directional properties of the aldehyde group.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿1,090.00 |
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| 5g | 10-20 days | ฿5,440.00 |
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| 25g | 10-20 days | ฿27,160.00 |
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5,6-Difluoro-o-anisaldehyde
Used in the synthesis of fluorinated organic compounds, particularly in pharmaceuticals and agrochemicals where fluorine substitution enhances metabolic stability and bioavailability. Serves as a building block in the preparation of active pharmaceutical ingredients (APIs) requiring difluorinated aromatic aldehydes. Its aldehyde and methoxy functional groups allow for versatile reactivity, including condensation and nucleophilic addition reactions. Commonly employed in the development of fluorinated analogs of biologically active molecules, such as kinase inhibitors or anti-inflammatory agents. Also utilized in materials science for constructing fluorinated liquid crystals or organic electronic materials due to the electron-withdrawing effect of fluorine atoms and the directional properties of the aldehyde group.
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