6-Chloro-4-phenyl-3-vinylquinolin-2(1H)-one
95%
- Product Code: 57087
CAS:
62452-22-6
| Molecular Weight: | 281.74 g./mol | Molecular Formula: | C₁₇H₁₂ClNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30472152 | |
| Melting Point: | 237-240 °C | Boiling Point: | 481.2±45.0 °C(Predicted) |
| Density: | 1.310±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
6-Chloro-4-phenyl-3-vinylquinolin-2(1H)-one is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the development of potential therapeutic agents, especially in the design of molecules targeting specific enzymes or receptors. This compound is often explored for its role in creating inhibitors or modulators for diseases such as cancer, inflammation, and neurological disorders. Additionally, its unique quinolinone core makes it a versatile scaffold for drug discovery, enabling researchers to modify its functional groups to enhance potency, selectivity, and pharmacokinetic properties. Beyond pharmaceuticals, it may also find applications in organic synthesis for constructing complex heterocyclic frameworks.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿9,360.00 |
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| 250mg | 10-20 days | ฿16,380.00 |
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| 1g | 10-20 days | ฿42,120.00 |
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6-Chloro-4-phenyl-3-vinylquinolin-2(1H)-one
6-Chloro-4-phenyl-3-vinylquinolin-2(1H)-one is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the development of potential therapeutic agents, especially in the design of molecules targeting specific enzymes or receptors. This compound is often explored for its role in creating inhibitors or modulators for diseases such as cancer, inflammation, and neurological disorders. Additionally, its unique quinolinone core makes it a versatile scaffold for drug discovery, enabling researchers to modify its functional groups to enhance potency, selectivity, and pharmacokinetic properties. Beyond pharmaceuticals, it may also find applications in organic synthesis for constructing complex heterocyclic frameworks.
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