5-Bromo-6-hydroxy-2-methylpyrimidin-4(1H)-one
≥95%
- Product Code: 116887
CAS:
4722-76-3
Molecular Weight: | 205.01 g./mol | Molecular Formula: | C₅H₅BrN₂O₂ |
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EC Number: | MDL Number: | MFCD18427081 | |
Melting Point: | Boiling Point: | 218°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various bioactive molecules, particularly those targeting enzyme inhibition. Its structural features make it valuable for designing compounds that interact with specific biological pathways, such as those involved in inflammation or cancer. Additionally, it is explored for its potential in creating novel antimicrobial agents, leveraging its pyrimidine core to disrupt microbial growth. Researchers also investigate its role in modifying nucleic acid analogs, which can be applied in antiviral therapies or genetic studies. Its versatility in organic synthesis further extends to the development of agrochemicals, where it contributes to the creation of new pesticides or herbicides.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | £37.05 |
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0.250 | 10-20 days | £61.68 |
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1.000 | 10-20 days | £184.83 |
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5-Bromo-6-hydroxy-2-methylpyrimidin-4(1H)-one
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various bioactive molecules, particularly those targeting enzyme inhibition. Its structural features make it valuable for designing compounds that interact with specific biological pathways, such as those involved in inflammation or cancer. Additionally, it is explored for its potential in creating novel antimicrobial agents, leveraging its pyrimidine core to disrupt microbial growth. Researchers also investigate its role in modifying nucleic acid analogs, which can be applied in antiviral therapies or genetic studies. Its versatility in organic synthesis further extends to the development of agrochemicals, where it contributes to the creation of new pesticides or herbicides.
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