1-(3-Fluoro-5-methoxyphenyl)ethan-1-amine
95%
- Product Code: 39285
CAS:
1270583-17-9
| Molecular Weight: | 169.2000 g./mol | Molecular Formula: | C₉H₁₂FNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18703526 | |
| 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 fluorine atom and a methoxy group, makes it a valuable building block for designing molecules with potential therapeutic effects. It is often employed in the development of drugs targeting the central nervous system, particularly those aimed at modulating neurotransmitter activity. Additionally, its unique chemical properties allow it to be incorporated into compounds being studied for their anti-inflammatory, analgesic, or antimicrobial properties. Researchers also explore its use in creating novel ligands for receptor-binding studies, aiding in the understanding of biological pathways and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿17,856.00 |
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1-(3-Fluoro-5-methoxyphenyl)ethan-1-amine
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 fluorine atom and a methoxy group, makes it a valuable building block for designing molecules with potential therapeutic effects. It is often employed in the development of drugs targeting the central nervous system, particularly those aimed at modulating neurotransmitter activity. Additionally, its unique chemical properties allow it to be incorporated into compounds being studied for their anti-inflammatory, analgesic, or antimicrobial properties. Researchers also explore its use in creating novel ligands for receptor-binding studies, aiding in the understanding of biological pathways and drug discovery.
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