1-(4-Fluorophenyl)propan-1-amine
95%
- Product Code: 59469
CAS:
74877-10-4
Molecular Weight: | 153.20 g./mol | Molecular Formula: | C₉H₁₂FN |
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EC Number: | MDL Number: | MFCD07186373 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, protected from light, stored under inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. It is particularly significant in the development of compounds that target the central nervous system, including potential antidepressants and anxiolytics. The presence of the fluorine atom enhances the molecule's binding affinity to specific receptors, making it a valuable building block in drug design. Additionally, it is explored in the creation of novel psychoactive substances, where its structural properties contribute to the modulation of neurotransmitter activity. Researchers also investigate its potential in the development of imaging agents for diagnostic purposes, leveraging its ability to interact with biological targets.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿8,964.00 |
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0.250 | 10-20 days | ฿13,446.00 |
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1.000 | 10-20 days | ฿33,615.00 |
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1-(4-Fluorophenyl)propan-1-amine
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. It is particularly significant in the development of compounds that target the central nervous system, including potential antidepressants and anxiolytics. The presence of the fluorine atom enhances the molecule's binding affinity to specific receptors, making it a valuable building block in drug design. Additionally, it is explored in the creation of novel psychoactive substances, where its structural properties contribute to the modulation of neurotransmitter activity. Researchers also investigate its potential in the development of imaging agents for diagnostic purposes, leveraging its ability to interact with biological targets.
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