tert-Butyl (7-bromoquinolin-4-yl)carbamate
95%
- Product Code: 37122
CAS:
1416438-99-7
| Molecular Weight: | 323.19 g./mol | Molecular Formula: | C₁₄H₁₅BrN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22690544 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Used in organic synthesis as an intermediate for the preparation of more complex quinoline derivatives. It is particularly valuable in pharmaceutical research, where it aids in the development of compounds with potential therapeutic properties. The bromine atom on the quinoline ring allows for further functionalization through cross-coupling reactions, making it a versatile building block in medicinal chemistry. Additionally, its tert-butyl carbamate group provides protection for amines during multi-step synthetic processes, ensuring selective reactions. This compound is also explored in the creation of fluorescent probes and materials for chemical sensing due to the inherent photophysical properties of the quinoline core.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,839.00 |
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tert-Butyl (7-bromoquinolin-4-yl)carbamate
Used in organic synthesis as an intermediate for the preparation of more complex quinoline derivatives. It is particularly valuable in pharmaceutical research, where it aids in the development of compounds with potential therapeutic properties. The bromine atom on the quinoline ring allows for further functionalization through cross-coupling reactions, making it a versatile building block in medicinal chemistry. Additionally, its tert-butyl carbamate group provides protection for amines during multi-step synthetic processes, ensuring selective reactions. This compound is also explored in the creation of fluorescent probes and materials for chemical sensing due to the inherent photophysical properties of the quinoline core.
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