Ethyl 5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylate
97%
- Product Code: 119962
CAS:
800401-67-6
| Molecular Weight: | 224.64 g./mol | Molecular Formula: | C₁₀H₉ClN₂O₂ |
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| EC Number: | MDL Number: | MFCD09878687 | |
| Melting Point: | Boiling Point: | 406°C at 760 mmHg | |
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its structure is valuable in the creation of biologically active compounds, often explored for potential therapeutic applications. Researchers focus on its role in developing drugs targeting specific diseases, such as neurological disorders or cancers, due to its pyrrolopyridine core, which is a common scaffold in medicinal chemistry. Additionally, it may be employed in the study of enzyme inhibition or receptor modulation, contributing to the discovery of novel treatments. Its applications are largely confined to laboratory settings, where it aids in advancing drug discovery efforts.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | €79.54 |
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| 0.250 | 10-20 days | €144.60 |
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| 1.000 | 10-20 days | €360.19 |
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| 5.000 | 10-20 days | €1,261.98 |
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Ethyl 5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylate
This compound is primarily utilized in pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its structure is valuable in the creation of biologically active compounds, often explored for potential therapeutic applications. Researchers focus on its role in developing drugs targeting specific diseases, such as neurological disorders or cancers, due to its pyrrolopyridine core, which is a common scaffold in medicinal chemistry. Additionally, it may be employed in the study of enzyme inhibition or receptor modulation, contributing to the discovery of novel treatments. Its applications are largely confined to laboratory settings, where it aids in advancing drug discovery efforts.
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