N'-Cyclooctylidene-4-methylbenzenesulfonohydrazide
95%
- Product Code: 215929
CAS:
2567-85-3
| Molecular Weight: | 294.41 g./mol | Molecular Formula: | C₁₅H₂₂N₂O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00086770 | |
| Melting Point: | 140 °C | Boiling Point: | 442.7±38.0 °C(Predicted) |
| Density: | 1.19±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, light-proof, inert gas |
Product Description:
Used primarily as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds. It serves as a key reagent in the development of hydrazone-based structures that exhibit biological activity, making it valuable in medicinal chemistry research. Its structure supports condensation reactions useful in forming nitrogen-containing rings, which are common in pharmaceuticals and agrochemicals. Additionally, it has been employed in studies involving cycloaddition reactions to construct complex cyclic frameworks. The compound’s stability and reactivity profile make it suitable for use in the synthesis of novel sulfonamide derivatives with potential antimicrobial or antitumor properties.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿2,640.00 |
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| 5g | 10-20 days | ฿9,230.00 |
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| 25g | 10-20 days | ฿34,970.00 |
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N'-Cyclooctylidene-4-methylbenzenesulfonohydrazide
Used primarily as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds. It serves as a key reagent in the development of hydrazone-based structures that exhibit biological activity, making it valuable in medicinal chemistry research. Its structure supports condensation reactions useful in forming nitrogen-containing rings, which are common in pharmaceuticals and agrochemicals. Additionally, it has been employed in studies involving cycloaddition reactions to construct complex cyclic frameworks. The compound’s stability and reactivity profile make it suitable for use in the synthesis of novel sulfonamide derivatives with potential antimicrobial or antitumor properties.
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