2-(Methylthio)pyrimidine-4,5,6-triamine
97%
- Product Code: 42055
CAS:
1431-40-9
| Molecular Weight: | 171.22 g./mol | Molecular Formula: | C₅H₉N₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00023239 | |
| Melting Point: | Boiling Point: | 451.3°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
2-(Methylthio)pyrimidine-4,5,6-triamine is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its structure makes it valuable for developing drugs that target specific biological pathways, particularly in the treatment of infections and certain types of cancers. The compound's pyrimidine core is often modified to create analogs that inhibit enzymes or interfere with nucleic acid synthesis, making it a crucial building block in drug discovery. Additionally, it finds application in agrochemical research for the development of herbicides and pesticides, where its derivatives can disrupt metabolic processes in target organisms. Its versatility in chemical synthesis also extends to the production of dyes and other specialty chemicals.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $176.29 |
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| 0.250 | 10-20 days | $352.59 |
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2-(Methylthio)pyrimidine-4,5,6-triamine
2-(Methylthio)pyrimidine-4,5,6-triamine is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its structure makes it valuable for developing drugs that target specific biological pathways, particularly in the treatment of infections and certain types of cancers. The compound's pyrimidine core is often modified to create analogs that inhibit enzymes or interfere with nucleic acid synthesis, making it a crucial building block in drug discovery. Additionally, it finds application in agrochemical research for the development of herbicides and pesticides, where its derivatives can disrupt metabolic processes in target organisms. Its versatility in chemical synthesis also extends to the production of dyes and other specialty chemicals.
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