1-(2-Chloropyrimidin-4-yl)-N-methylpiperidin-3-amine hydrochloride
95%
- Product Code: 59450
CAS:
1289387-24-1
| Molecular Weight: | 263.17 g./mol | Molecular Formula: | C₁₀H₁₆Cl₂N₄ |
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| EC Number: | MDL Number: | MFCD18837526 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring a chloropyrimidine moiety, makes it a valuable building block for developing compounds that target specific enzymes or receptors, particularly in the context of kinase inhibition. It is often employed in the design and optimization of drug candidates for therapeutic areas such as oncology, where kinase inhibitors play a crucial role in disrupting signaling pathways involved in cancer progression. Additionally, its piperidine ring contributes to enhancing the bioavailability and binding affinity of the resulting drug molecules, making it a versatile scaffold in drug discovery efforts. Researchers also leverage its reactivity in coupling reactions to create diverse chemical libraries for high-throughput screening, aiding in the identification of novel bioactive compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿10,665.00 |
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1-(2-Chloropyrimidin-4-yl)-N-methylpiperidin-3-amine hydrochloride
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring a chloropyrimidine moiety, makes it a valuable building block for developing compounds that target specific enzymes or receptors, particularly in the context of kinase inhibition. It is often employed in the design and optimization of drug candidates for therapeutic areas such as oncology, where kinase inhibitors play a crucial role in disrupting signaling pathways involved in cancer progression. Additionally, its piperidine ring contributes to enhancing the bioavailability and binding affinity of the resulting drug molecules, making it a versatile scaffold in drug discovery efforts. Researchers also leverage its reactivity in coupling reactions to create diverse chemical libraries for high-throughput screening, aiding in the identification of novel bioactive compounds.
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