1-(3-Fluoro-4-methylphenyl)ethanamine hydrochloride
95%
- Product Code: 39282
CAS:
2138165-91-8
| Molecular Weight: | 189.6576 g./mol | Molecular Formula: | C₉H₁₃ClFN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31421008 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure, featuring a fluoro and methyl substituent on the phenyl ring, makes it valuable for designing molecules with specific biological activities. It is often employed in the development of central nervous system (CNS) drugs, particularly those targeting neurological disorders such as depression, anxiety, or Parkinson's disease. The presence of the fluorine atom enhances the compound's ability to interact with biological targets, improving the pharmacokinetic properties of the resulting drugs. Additionally, it is used in research to study receptor-binding interactions and to optimize drug candidates for better efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿12,456.00 |
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1-(3-Fluoro-4-methylphenyl)ethanamine hydrochloride
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure, featuring a fluoro and methyl substituent on the phenyl ring, makes it valuable for designing molecules with specific biological activities. It is often employed in the development of central nervous system (CNS) drugs, particularly those targeting neurological disorders such as depression, anxiety, or Parkinson's disease. The presence of the fluorine atom enhances the compound's ability to interact with biological targets, improving the pharmacokinetic properties of the resulting drugs. Additionally, it is used in research to study receptor-binding interactions and to optimize drug candidates for better efficacy and selectivity.
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