6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride
98.0%
- Product Code: 120392
CAS:
2328-12-3
| Molecular Weight: | 229.7 g./mol | Molecular Formula: | C₁₁H₁₆ClNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00012744 | |
| Melting Point: | 260-265 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in pharmacological research due to its structural similarity to certain alkaloids. It serves as a key intermediate in the synthesis of various bioactive molecules, particularly those targeting the central nervous system. Researchers use it to develop potential therapeutic agents for neurological disorders, such as Parkinson's disease and depression, owing to its ability to interact with neurotransmitter systems. Additionally, it is employed in studies exploring the mechanisms of action of isoquinoline derivatives, which are known for their diverse biological activities. Its hydrochloride form enhances solubility, making it more suitable for experimental applications in aqueous solutions.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 98 |
| Purity (Titration With AgNO3) | 97.5-102.5 |
| Appearance | White To Light Yellow Powder |
| Infrared Spectrometry | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $15.30 |
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| 25.000 | 10-20 days | $58.21 |
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| 100.000 | 10-20 days | $191.42 |
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| 500.000 | 10-20 days | $859.89 |
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6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride
This compound is primarily utilized in pharmacological research due to its structural similarity to certain alkaloids. It serves as a key intermediate in the synthesis of various bioactive molecules, particularly those targeting the central nervous system. Researchers use it to develop potential therapeutic agents for neurological disorders, such as Parkinson's disease and depression, owing to its ability to interact with neurotransmitter systems. Additionally, it is employed in studies exploring the mechanisms of action of isoquinoline derivatives, which are known for their diverse biological activities. Its hydrochloride form enhances solubility, making it more suitable for experimental applications in aqueous solutions.
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