3-Bromo-pyrrolo[1,2-a]pyrimidine-6-carboxylic acid ethyl ester
96%
- Product Code: 45348
CAS:
2097068-59-0
| Molecular Weight: | 269.0947 g./mol | Molecular Formula: | C₁₀H₉BrN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30735885 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex molecules. It is often employed in pharmaceutical research, particularly in the design and synthesis of drug candidates targeting various biological pathways. Its pyrrolo[1,2-a]pyrimidine core structure is valuable in medicinal chemistry for creating compounds with potential therapeutic properties, such as kinase inhibitors or anti-inflammatory agents. Additionally, it can serve as a building block in the synthesis of heterocyclic compounds, which are widely explored for their biological activities. Its ethyl ester group also allows for further functionalization, making it a useful precursor in chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $512.05 |
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3-Bromo-pyrrolo[1,2-a]pyrimidine-6-carboxylic acid ethyl ester
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex molecules. It is often employed in pharmaceutical research, particularly in the design and synthesis of drug candidates targeting various biological pathways. Its pyrrolo[1,2-a]pyrimidine core structure is valuable in medicinal chemistry for creating compounds with potential therapeutic properties, such as kinase inhibitors or anti-inflammatory agents. Additionally, it can serve as a building block in the synthesis of heterocyclic compounds, which are widely explored for their biological activities. Its ethyl ester group also allows for further functionalization, making it a useful precursor in chemical transformations.
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