tert-Butyl N-[1-(4-bromophenyl)-3-oxocyclobutyl]carbamate
97%
- Product Code: 121452
CAS:
1199556-68-7
| Molecular Weight: | 340.21 g./mol | Molecular Formula: | C₁₅H₁₈BrNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17926307 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its structure, featuring a bromophenyl group and a cyclobutyl ring, makes it a valuable intermediate for constructing complex chemical frameworks. It is often employed in the synthesis of potential drug candidates, especially those targeting neurological or inflammatory disorders, due to its ability to interact with specific biological pathways. Additionally, it serves as a precursor in the preparation of compounds for research in medicinal chemistry, aiding in the exploration of new therapeutic agents. Its stability and reactivity make it suitable for use in multi-step synthetic processes, enabling the creation of diverse molecular architectures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,483.00 |
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| 0.250 | 10-20 days | ฿5,580.00 |
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| 1.000 | 10-20 days | ฿10,845.00 |
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tert-Butyl N-[1-(4-bromophenyl)-3-oxocyclobutyl]carbamate
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its structure, featuring a bromophenyl group and a cyclobutyl ring, makes it a valuable intermediate for constructing complex chemical frameworks. It is often employed in the synthesis of potential drug candidates, especially those targeting neurological or inflammatory disorders, due to its ability to interact with specific biological pathways. Additionally, it serves as a precursor in the preparation of compounds for research in medicinal chemistry, aiding in the exploration of new therapeutic agents. Its stability and reactivity make it suitable for use in multi-step synthetic processes, enabling the creation of diverse molecular architectures.
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