(2-Amino-6-fluorophenyl)methanol
95%
- Product Code: 74199
CAS:
221285-25-2
| Molecular Weight: | 141.14 g./mol | Molecular Formula: | C₇H₈FNO |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
(2-Amino-6-fluorophenyl)methanol is primarily used in the synthesis of pharmaceuticals and organic compounds. It serves as a key intermediate in the production of various drugs, particularly those targeting neurological and psychiatric conditions. Its structure allows for the development of molecules with specific biological activities, making it valuable in medicinal chemistry. Additionally, it is utilized in research for creating novel compounds with potential therapeutic applications. The presence of both amino and hydroxyl groups in its structure enables diverse chemical modifications, facilitating its role in the development of new drug candidates.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Pale-yellow to Yellow-brown Solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.050 | 10-20 days | $21.09 |
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| 0.250 | 10-20 days | $49.72 |
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| 1.000 | 10-20 days | $179.81 |
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| 5.000 | 10-20 days | $778.50 |
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(2-Amino-6-fluorophenyl)methanol
(2-Amino-6-fluorophenyl)methanol is primarily used in the synthesis of pharmaceuticals and organic compounds. It serves as a key intermediate in the production of various drugs, particularly those targeting neurological and psychiatric conditions. Its structure allows for the development of molecules with specific biological activities, making it valuable in medicinal chemistry. Additionally, it is utilized in research for creating novel compounds with potential therapeutic applications. The presence of both amino and hydroxyl groups in its structure enables diverse chemical modifications, facilitating its role in the development of new drug candidates.
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