4-((4-Amino-6-chloropyrimidin-2-yl)amino)benzonitrile
≥95%
- Product Code: 81179
CAS:
1398507-08-8
| Molecular Weight: | 245.67 g./mol | Molecular Formula: | C₁₁H₈ClN₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD24682776 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This chemical is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting specific enzyme pathways. Its structural features make it valuable for designing molecules with potential therapeutic applications, such as inhibitors for certain kinases or receptors involved in disease mechanisms. Researchers often employ it in the creation of novel drug candidates, especially in areas like oncology and inflammation, where precise molecular interactions are crucial. Additionally, it may be used in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of new drugs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,552.00 |
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| 0.250 | 10-20 days | ฿13,095.00 |
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4-((4-Amino-6-chloropyrimidin-2-yl)amino)benzonitrile
This chemical is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting specific enzyme pathways. Its structural features make it valuable for designing molecules with potential therapeutic applications, such as inhibitors for certain kinases or receptors involved in disease mechanisms. Researchers often employ it in the creation of novel drug candidates, especially in areas like oncology and inflammation, where precise molecular interactions are crucial. Additionally, it may be used in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of new drugs.
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