1-N-Boc-3-Fluoro-Aniline
97%
- Product Code: 69183
CAS:
81740-18-3
| Molecular Weight: | 211.24 g./mol | Molecular Formula: | C₁₁H₁₄FNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 231.6ºC | |
| Density: | 1.156g/cm3 | Storage Condition: | room temperature, dry |
Product Description:
1-N-Boc-3-Fluoro-Aniline is widely used in organic synthesis, particularly in the pharmaceutical industry, as a key intermediate for the development of various active pharmaceutical ingredients (APIs). Its Boc-protected amine group allows for selective reactions, making it valuable in multi-step synthesis processes. The fluorine atom enhances the biological activity and metabolic stability of the final compounds, making it a preferred choice in drug discovery. It is also employed in the synthesis of agrochemicals and specialty chemicals, where its unique structure contributes to the development of compounds with specific properties. Additionally, it serves as a building block in the preparation of fluorinated aromatic compounds, which are essential in materials science and advanced research applications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Yellow Solid |
| PURITY | 96.5-100 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,530.00 |
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| 5.000 | 10-20 days | ฿6,690.00 |
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1-N-Boc-3-Fluoro-Aniline
1-N-Boc-3-Fluoro-Aniline is widely used in organic synthesis, particularly in the pharmaceutical industry, as a key intermediate for the development of various active pharmaceutical ingredients (APIs). Its Boc-protected amine group allows for selective reactions, making it valuable in multi-step synthesis processes. The fluorine atom enhances the biological activity and metabolic stability of the final compounds, making it a preferred choice in drug discovery. It is also employed in the synthesis of agrochemicals and specialty chemicals, where its unique structure contributes to the development of compounds with specific properties. Additionally, it serves as a building block in the preparation of fluorinated aromatic compounds, which are essential in materials science and advanced research applications.
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