6-Chloro-2-fluoropyridine-3-carboxaldehyde
95%
- Product Code: 49537
CAS:
1093880-37-5
| Molecular Weight: | 159.5455232 g./mol | Molecular Formula: | C₆H₃ClFNO |
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| EC Number: | MDL Number: | ||
| Melting Point: | 49-50 ℃(Solv: hexane (110-54-3)) | Boiling Point: | 255.5±35.0 ℃(Predicted) |
| Density: | 1.444±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex molecules. Its structure, featuring both chloro and fluoro substituents, makes it a versatile building block for constructing heterocyclic compounds. In pharmaceutical research, it is often employed in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce specific functional groups into target molecules. Additionally, it finds application in the creation of agrochemicals, where it contributes to the synthesis of herbicides, insecticides, and fungicides. Its reactivity and stability under various conditions make it a valuable component in organic synthesis, particularly in the formation of pyridine derivatives.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿11,052.00 |
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| 1.000 | 10-20 days | ฿29,052.00 |
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6-Chloro-2-fluoropyridine-3-carboxaldehyde
This compound is primarily utilized in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex molecules. Its structure, featuring both chloro and fluoro substituents, makes it a versatile building block for constructing heterocyclic compounds. In pharmaceutical research, it is often employed in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce specific functional groups into target molecules. Additionally, it finds application in the creation of agrochemicals, where it contributes to the synthesis of herbicides, insecticides, and fungicides. Its reactivity and stability under various conditions make it a valuable component in organic synthesis, particularly in the formation of pyridine derivatives.
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