(S)-tert-Butyl 1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride
97%
- Product Code: 113636
CAS:
82586-60-5
| Molecular Weight: | 269.77 g./mol | Molecular Formula: | C₁₄H₂₀ClNO₂ |
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| EC Number: | MDL Number: | MFCD00672723 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral intermediates. It serves as a key building block in the production of various biologically active molecules, including potential drug candidates targeting neurological disorders. Its chiral nature makes it valuable for creating enantiomerically pure compounds, which are essential for studying structure-activity relationships in medicinal chemistry. Additionally, it is employed in the preparation of tetrahydroisoquinoline derivatives, which are known for their diverse pharmacological properties, such as antitumor, antimicrobial, and cardiovascular activities. The hydrochloride salt form enhances its stability and solubility, facilitating its use in experimental and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $116.24 |
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| 1.000 | 10-20 days | $233.32 |
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| 5.000 | 10-20 days | $630.63 |
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(S)-tert-Butyl 1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral intermediates. It serves as a key building block in the production of various biologically active molecules, including potential drug candidates targeting neurological disorders. Its chiral nature makes it valuable for creating enantiomerically pure compounds, which are essential for studying structure-activity relationships in medicinal chemistry. Additionally, it is employed in the preparation of tetrahydroisoquinoline derivatives, which are known for their diverse pharmacological properties, such as antitumor, antimicrobial, and cardiovascular activities. The hydrochloride salt form enhances its stability and solubility, facilitating its use in experimental and industrial applications.
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