6-Bromoquinazoline-4-carbonitrile
97%
- Product Code: 81537
CAS:
1204334-27-9
| Molecular Weight: | 234.06 g./mol | Molecular Formula: | C₉H₄BrN₃ |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the pharmaceutical and chemical research industries as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of quinazoline-based compounds, which are known for their potential therapeutic applications. It serves as a building block in the creation of inhibitors targeting specific enzymes, such as tyrosine kinases, which play a critical role in cell signaling and cancer progression. Additionally, it is employed in the preparation of compounds with potential anti-inflammatory, antiviral, and antimicrobial properties, making it a versatile tool in drug discovery and development. Its reactive bromo and cyano groups allow for further functionalization, enabling the design of diverse chemical libraries for screening and optimization.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿4,203.00 |
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| 0.250 | 10-20 days | ฿12,672.00 |
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6-Bromoquinazoline-4-carbonitrile
This compound is primarily utilized in the pharmaceutical and chemical research industries as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of quinazoline-based compounds, which are known for their potential therapeutic applications. It serves as a building block in the creation of inhibitors targeting specific enzymes, such as tyrosine kinases, which play a critical role in cell signaling and cancer progression. Additionally, it is employed in the preparation of compounds with potential anti-inflammatory, antiviral, and antimicrobial properties, making it a versatile tool in drug discovery and development. Its reactive bromo and cyano groups allow for further functionalization, enabling the design of diverse chemical libraries for screening and optimization.
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