5'-Bromospiro[1,3-dioxolane-2,3'-indol]-2'(1'H)-one
99%
- Product Code: 75641
CAS:
75822-54-7
| Molecular Weight: | 270.081 g./mol | Molecular Formula: | C₁₀H₈BrNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00097597 | |
| Melting Point: | Boiling Point: | 451.2℃ at 760 mmHg | |
| Density: | 1.81g/ml | Storage Condition: | Room temperature, sealed, ventilated |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules, particularly in pharmaceutical research. Its structure, featuring both a bromine atom and a spirocyclic indole moiety, makes it valuable for constructing biologically active compounds, such as potential drug candidates targeting neurological disorders or cancer. The bromine atom serves as a reactive site for further functionalization through cross-coupling reactions, enabling the introduction of diverse substituents. Additionally, the spirocyclic framework can contribute to the stability and specificity of the resulting molecules, enhancing their potential therapeutic efficacy. Researchers also explore its use in the synthesis of novel heterocyclic compounds, which are often investigated for their pharmacological properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,620.00 |
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| 1.000 | 10-20 days | ฿5,850.00 |
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5'-Bromospiro[1,3-dioxolane-2,3'-indol]-2'(1'H)-one
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules, particularly in pharmaceutical research. Its structure, featuring both a bromine atom and a spirocyclic indole moiety, makes it valuable for constructing biologically active compounds, such as potential drug candidates targeting neurological disorders or cancer. The bromine atom serves as a reactive site for further functionalization through cross-coupling reactions, enabling the introduction of diverse substituents. Additionally, the spirocyclic framework can contribute to the stability and specificity of the resulting molecules, enhancing their potential therapeutic efficacy. Researchers also explore its use in the synthesis of novel heterocyclic compounds, which are often investigated for their pharmacological properties.
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