Methyl 5-bromo-1H-indazole-4-carboxylate
95%
- Product Code: 48862
CAS:
1037840-79-1
| Molecular Weight: | 255.0681 g./mol | Molecular Formula: | C₉H₇BrN₂O₂ |
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| EC Number: | MDL Number: | MFCD13177017 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
Methyl 5-bromo-1H-indazole-4-carboxylate is primarily used in the field of organic synthesis, particularly as a key intermediate in the development of pharmaceuticals. Its structure is valuable for constructing more complex molecules, especially those with potential biological activity.
In medicinal chemistry, it serves as a building block for designing and synthesizing novel compounds targeting various diseases. For instance, it can be incorporated into the development of inhibitors for specific enzymes or receptors, which may have applications in treating cancer, inflammation, or neurological disorders.
Additionally, its bromo and ester functional groups make it a versatile reagent for further chemical modifications, such as cross-coupling reactions or nucleophilic substitutions, enabling the creation of diverse chemical libraries for drug discovery. Its role in research and development underscores its importance in advancing therapeutic innovations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £76.54 |
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Methyl 5-bromo-1H-indazole-4-carboxylate
Methyl 5-bromo-1H-indazole-4-carboxylate is primarily used in the field of organic synthesis, particularly as a key intermediate in the development of pharmaceuticals. Its structure is valuable for constructing more complex molecules, especially those with potential biological activity.
In medicinal chemistry, it serves as a building block for designing and synthesizing novel compounds targeting various diseases. For instance, it can be incorporated into the development of inhibitors for specific enzymes or receptors, which may have applications in treating cancer, inflammation, or neurological disorders.
Additionally, its bromo and ester functional groups make it a versatile reagent for further chemical modifications, such as cross-coupling reactions or nucleophilic substitutions, enabling the creation of diverse chemical libraries for drug discovery. Its role in research and development underscores its importance in advancing therapeutic innovations.
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