3-(2-Chlorophenyl)-6-Fluoro-2-Methyl-4(3H)-Quinazolinone
95%
- Product Code: 82449
CAS:
49579-12-6
| Molecular Weight: | 288.70 g./mol | Molecular Formula: | C₁₅H₁₀ClFN₂O |
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| EC Number: | MDL Number: | MFCD01686277 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structural framework is particularly valuable in the development of quinazoline derivatives, which are known for their diverse biological activities. Specifically, it has been explored for its potential role in creating compounds with anti-inflammatory, anticancer, and antimicrobial properties. Researchers have also investigated its use in designing molecules that can inhibit specific enzymes or receptors, making it a promising candidate for drug discovery programs targeting diseases such as cancer and inflammatory disorders. Additionally, its fluorinated and chlorinated aromatic components contribute to its stability and bioavailability, enhancing its efficacy in therapeutic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $631.66 |
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| 0.250 | 10-20 days | $1,068.96 |
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| 1.000 | 10-20 days | $2,167.81 |
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3-(2-Chlorophenyl)-6-Fluoro-2-Methyl-4(3H)-Quinazolinone
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structural framework is particularly valuable in the development of quinazoline derivatives, which are known for their diverse biological activities. Specifically, it has been explored for its potential role in creating compounds with anti-inflammatory, anticancer, and antimicrobial properties. Researchers have also investigated its use in designing molecules that can inhibit specific enzymes or receptors, making it a promising candidate for drug discovery programs targeting diseases such as cancer and inflammatory disorders. Additionally, its fluorinated and chlorinated aromatic components contribute to its stability and bioavailability, enhancing its efficacy in therapeutic applications.
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