tert-Butyl 7-chloro-5-nitro-3H-imidazo[4,5-b]pyridine-3-carboxylate
95%
- Product Code: 120843
CAS:
878011-44-0
| Molecular Weight: | 298.68 g./mol | Molecular Formula: | C₁₁H₁₁ClN₄O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13183293 | |
| Melting Point: | Boiling Point: | 431.6±55.0 °C(Predicted) | |
| Density: | 1.53±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, inert gas |
Product Description:
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the creation of compounds targeting specific enzymes or receptors, often in the context of drug discovery for treating diseases such as cancer or infections. Additionally, it serves as a building block in the preparation of complex heterocyclic compounds, which are essential in medicinal chemistry for designing novel therapeutic agents. Its nitro and chloro functional groups make it a versatile precursor for further chemical modifications, enabling the development of diverse drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €229.60 |
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| 0.250 | 10-20 days | €390.11 |
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| 1.000 | 10-20 days | €1,053.04 |
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tert-Butyl 7-chloro-5-nitro-3H-imidazo[4,5-b]pyridine-3-carboxylate
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the creation of compounds targeting specific enzymes or receptors, often in the context of drug discovery for treating diseases such as cancer or infections. Additionally, it serves as a building block in the preparation of complex heterocyclic compounds, which are essential in medicinal chemistry for designing novel therapeutic agents. Its nitro and chloro functional groups make it a versatile precursor for further chemical modifications, enabling the development of diverse drug candidates.
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