(4-Bromo-benzothiazol-2-yl)-carbamic acid tert-butyl ester
95%
- Product Code: 36928
CAS:
1823565-33-8
| Molecular Weight: | 329.2128 g./mol | Molecular Formula: | C₁₂H₁₃BrN₂O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28154577 | |
| 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 development of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a bromo-benzothiazole moiety, makes it valuable for constructing heterocyclic compounds that are often explored for their biological activities. It is commonly employed in the synthesis of potential drug candidates, especially those targeting neurological disorders or cancer, due to the benzothiazole scaffold's relevance in medicinal chemistry. Additionally, it serves as a building block in the preparation of compounds for agrochemical research, where benzothiazole derivatives are investigated for their pesticidal or herbicidal properties. The tert-butyl ester group in the molecule provides stability and facilitates further functionalization during synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,862.00 |
+
-
|
(4-Bromo-benzothiazol-2-yl)-carbamic acid tert-butyl ester
This compound is primarily utilized in organic synthesis as a key intermediate in the development of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a bromo-benzothiazole moiety, makes it valuable for constructing heterocyclic compounds that are often explored for their biological activities. It is commonly employed in the synthesis of potential drug candidates, especially those targeting neurological disorders or cancer, due to the benzothiazole scaffold's relevance in medicinal chemistry. Additionally, it serves as a building block in the preparation of compounds for agrochemical research, where benzothiazole derivatives are investigated for their pesticidal or herbicidal properties. The tert-butyl ester group in the molecule provides stability and facilitates further functionalization during synthetic processes.
| 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 :