2-(3-Bromophenyl)-4-phenylquinazoline
98%
- Product Code: 41512
CAS:
1149343-61-2
| Molecular Weight: | 361.23462 g./mol | Molecular Formula: | C₂₀H₁₃BrN₂ |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
2-(3-Bromophenyl)-4-phenylquinazoline is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting cancer therapy. The quinazoline core structure is known for its potential in inhibiting enzymes like tyrosine kinases, which play a critical role in cell signaling and cancer progression. This compound is often explored for its ability to modulate these pathways, making it valuable in the development of novel anticancer agents. Additionally, it is studied for its potential applications in designing drugs for other diseases where enzyme inhibition is a therapeutic strategy. Its structural features allow for further chemical modifications to enhance efficacy and selectivity in drug discovery efforts.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,364.00 |
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| 1.000 | 10-20 days | ฿7,848.00 |
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| 5.000 | 10-20 days | ฿28,791.00 |
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2-(3-Bromophenyl)-4-phenylquinazoline
2-(3-Bromophenyl)-4-phenylquinazoline is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting cancer therapy. The quinazoline core structure is known for its potential in inhibiting enzymes like tyrosine kinases, which play a critical role in cell signaling and cancer progression. This compound is often explored for its ability to modulate these pathways, making it valuable in the development of novel anticancer agents. Additionally, it is studied for its potential applications in designing drugs for other diseases where enzyme inhibition is a therapeutic strategy. Its structural features allow for further chemical modifications to enhance efficacy and selectivity in drug discovery efforts.
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