(3-Fluoro-4-((tetrahydro-2H-pyran-4-yl)oxy)phenyl)methanamine
97%
- Product Code: 36653
CAS:
1247619-84-6
| Molecular Weight: | 225.2594 g./mol | Molecular Formula: | C₁₂H₁₆FNO₂ |
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| EC Number: | MDL Number: | MFCD14614843 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the design and synthesis of novel drug candidates. Its structure, featuring a fluorine atom and a tetrahydro-2H-pyran-4-yloxy group, makes it a valuable intermediate for creating molecules with potential therapeutic properties. It is often explored in the development of central nervous system (CNS) drugs due to its ability to cross the blood-brain barrier. Additionally, it may be used in the study of receptor interactions and enzyme inhibition, contributing to the discovery of treatments for neurological disorders, psychiatric conditions, or other diseases. Its unique chemical properties also make it a candidate for further modification in medicinal chemistry to enhance drug efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $392.37 |
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(3-Fluoro-4-((tetrahydro-2H-pyran-4-yl)oxy)phenyl)methanamine
This compound is primarily utilized in pharmaceutical research and development, particularly in the design and synthesis of novel drug candidates. Its structure, featuring a fluorine atom and a tetrahydro-2H-pyran-4-yloxy group, makes it a valuable intermediate for creating molecules with potential therapeutic properties. It is often explored in the development of central nervous system (CNS) drugs due to its ability to cross the blood-brain barrier. Additionally, it may be used in the study of receptor interactions and enzyme inhibition, contributing to the discovery of treatments for neurological disorders, psychiatric conditions, or other diseases. Its unique chemical properties also make it a candidate for further modification in medicinal chemistry to enhance drug efficacy and selectivity.
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