tert-Butyl 6-(bromomethyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate
95%
- Product Code: 49509
CAS:
622867-53-2
| Molecular Weight: | 326.2300 g./mol | Molecular Formula: | C₁₅H₂₀BrNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12408125 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules, particularly in pharmaceutical research. Its structure, featuring both a bromomethyl group and a protected amine, makes it valuable for constructing isoquinoline derivatives, which are often explored for their biological activities. The bromomethyl group allows for further functionalization through nucleophilic substitution reactions, enabling the attachment of various substituents. Additionally, the tert-butyloxycarbonyl (Boc) protecting group can be selectively removed under mild conditions, providing access to the free amine for further modifications. This makes it a versatile building block in the development of potential drug candidates, especially in the synthesis of compounds targeting neurological or cardiovascular disorders.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿13,545.00 |
+
-
|
tert-Butyl 6-(bromomethyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate
This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules, particularly in pharmaceutical research. Its structure, featuring both a bromomethyl group and a protected amine, makes it valuable for constructing isoquinoline derivatives, which are often explored for their biological activities. The bromomethyl group allows for further functionalization through nucleophilic substitution reactions, enabling the attachment of various substituents. Additionally, the tert-butyloxycarbonyl (Boc) protecting group can be selectively removed under mild conditions, providing access to the free amine for further modifications. This makes it a versatile building block in the development of potential drug candidates, especially in the synthesis of compounds targeting neurological or cardiovascular disorders.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
฿0.00
฿0.00
Total :