(S)-4-Fluoro-2,3-dihydro-1H-inden-1-amine hydrochloride
≥95%
- Product Code: 113817
CAS:
1286734-90-4
| Molecular Weight: | 187.64 g./mol | Molecular Formula: | C₉H₁₁ClFN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16295140 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
(S)-4-Fluoro-2,3-dihydro-1H-inden-1-amine hydrochloride is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate or building block in the synthesis of various biologically active compounds. Its structure, featuring a fluorinated indane core, makes it valuable for developing potential drug candidates, particularly in the design of central nervous system (CNS) targeting agents. Researchers explore its application in creating molecules with potential antidepressant, antipsychotic, or anxiolytic properties due to its ability to interact with neurotransmitter systems. Additionally, its chiral nature allows for the study of enantioselective interactions in drug-receptor binding, contributing to the development of more effective and targeted therapies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,797.00 |
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| 0.250 | 10-20 days | ฿7,740.00 |
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| 1.000 | 10-20 days | ฿19,368.00 |
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(S)-4-Fluoro-2,3-dihydro-1H-inden-1-amine hydrochloride
(S)-4-Fluoro-2,3-dihydro-1H-inden-1-amine hydrochloride is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate or building block in the synthesis of various biologically active compounds. Its structure, featuring a fluorinated indane core, makes it valuable for developing potential drug candidates, particularly in the design of central nervous system (CNS) targeting agents. Researchers explore its application in creating molecules with potential antidepressant, antipsychotic, or anxiolytic properties due to its ability to interact with neurotransmitter systems. Additionally, its chiral nature allows for the study of enantioselective interactions in drug-receptor binding, contributing to the development of more effective and targeted therapies.
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