1-Propyl-1,2,3,4-tetrahydroquinolin-7-amine
98%
- Product Code: 71745
CAS:
1049677-37-3
| Molecular Weight: | 190.29 g./mol | Molecular Formula: | C₁₂H₁₈N₂ |
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| EC Number: | MDL Number: | MFCD11053458 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry due to its structural properties, which make it a valuable intermediate in the synthesis of various pharmacologically active molecules. It is often explored for its potential in developing central nervous system (CNS) drugs, particularly those targeting neurological disorders such as depression, anxiety, and neurodegenerative diseases. The tetrahydroquinoline core of the compound is known for its ability to interact with biological targets like receptors or enzymes, making it a promising scaffold for drug discovery. Additionally, its amine functionality allows for further chemical modifications, enabling the creation of derivatives with enhanced biological activity or improved pharmacokinetic properties. Researchers also investigate its role in designing compounds with potential anti-inflammatory or antimicrobial effects, broadening its applicability in therapeutic development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | $79.12 |
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| 0.100 | 10-20 days | $191.45 |
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1-Propyl-1,2,3,4-tetrahydroquinolin-7-amine
This compound is primarily utilized in the field of medicinal chemistry due to its structural properties, which make it a valuable intermediate in the synthesis of various pharmacologically active molecules. It is often explored for its potential in developing central nervous system (CNS) drugs, particularly those targeting neurological disorders such as depression, anxiety, and neurodegenerative diseases. The tetrahydroquinoline core of the compound is known for its ability to interact with biological targets like receptors or enzymes, making it a promising scaffold for drug discovery. Additionally, its amine functionality allows for further chemical modifications, enabling the creation of derivatives with enhanced biological activity or improved pharmacokinetic properties. Researchers also investigate its role in designing compounds with potential anti-inflammatory or antimicrobial effects, broadening its applicability in therapeutic development.
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