N-(tert-Butyl)-6-chloro-4-(o-tolyl)nicotinamide
97%
- Product Code: 124819
CAS:
342417-04-3
| Molecular Weight: | 302.80 g./mol | Molecular Formula: | C₁₇H₁₉ClN₂O |
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| EC Number: | MDL Number: | MFCD09032565 | |
| Melting Point: | Boiling Point: | 429.4±45.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules. It is often employed in the development of pharmaceutical agents, particularly those targeting specific enzymes or receptors in the body. Its structure, featuring a nicotinamide core, makes it a valuable building block for creating compounds with potential therapeutic effects, such as anti-inflammatory, anticancer, or antiviral properties. Researchers also explore its use in designing inhibitors for various biological pathways, contributing to drug discovery and development efforts. Additionally, its chemical properties allow for further functionalization, enabling the creation of derivatives with enhanced biological activity or selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $15.70 |
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| 1.000 | 10-20 days | $45.23 |
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N-(tert-Butyl)-6-chloro-4-(o-tolyl)nicotinamide
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules. It is often employed in the development of pharmaceutical agents, particularly those targeting specific enzymes or receptors in the body. Its structure, featuring a nicotinamide core, makes it a valuable building block for creating compounds with potential therapeutic effects, such as anti-inflammatory, anticancer, or antiviral properties. Researchers also explore its use in designing inhibitors for various biological pathways, contributing to drug discovery and development efforts. Additionally, its chemical properties allow for further functionalization, enabling the creation of derivatives with enhanced biological activity or selectivity.
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