6-Fluoro-2-(prop-1-en-2-yl)benzo[d]oxazole
95%
- Product Code: 87638
CAS:
1373278-76-2
| Molecular Weight: | 177.18 g./mol | Molecular Formula: | C₁₀H₈FNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28681041 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry, dark |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex molecules. Its structure, featuring a benzo[d]oxazole core with a fluoro substituent and a prop-1-en-2-yl group, makes it valuable in the construction of pharmaceuticals, particularly in the synthesis of potential drug candidates targeting various biological pathways. Additionally, it finds application in material science, where it can be incorporated into the design of organic electronic materials, such as light-emitting diodes (LEDs) or organic semiconductors, due to its electron-rich aromatic system. The presence of the fluoro group also enhances its reactivity, making it a useful building block in the development of agrochemicals and specialty chemicals.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,430.00 |
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| 0.250 | 10-20 days | ฿4,563.00 |
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6-Fluoro-2-(prop-1-en-2-yl)benzo[d]oxazole
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex molecules. Its structure, featuring a benzo[d]oxazole core with a fluoro substituent and a prop-1-en-2-yl group, makes it valuable in the construction of pharmaceuticals, particularly in the synthesis of potential drug candidates targeting various biological pathways. Additionally, it finds application in material science, where it can be incorporated into the design of organic electronic materials, such as light-emitting diodes (LEDs) or organic semiconductors, due to its electron-rich aromatic system. The presence of the fluoro group also enhances its reactivity, making it a useful building block in the development of agrochemicals and specialty chemicals.
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