4-Amino-8-bromo-2-chloroquinazoline
97%
- Product Code: 104597
CAS:
956100-62-2
| Molecular Weight: | 258.51 g./mol | Molecular Formula: | C₈H₅BrClN₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11858275 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure makes it a valuable intermediate in the creation of quinazoline derivatives, which are often explored for their potential therapeutic properties. Researchers focus on its application in designing molecules that target specific enzymes or receptors, particularly in the fields of oncology and infectious diseases. Additionally, it serves as a building block in medicinal chemistry for developing compounds with potential anti-cancer, anti-inflammatory, or antimicrobial activities. Its halogenated and amino-functionalized structure allows for further chemical modifications, enabling the exploration of diverse biological activities.
Product Specification:
| Test | Specification |
|---|---|
| Purity (%) | 96.5-100 |
| Appearance | Solid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,521.00 |
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| 5.000 | 10-20 days | ฿5,382.00 |
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4-Amino-8-bromo-2-chloroquinazoline
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure makes it a valuable intermediate in the creation of quinazoline derivatives, which are often explored for their potential therapeutic properties. Researchers focus on its application in designing molecules that target specific enzymes or receptors, particularly in the fields of oncology and infectious diseases. Additionally, it serves as a building block in medicinal chemistry for developing compounds with potential anti-cancer, anti-inflammatory, or antimicrobial activities. Its halogenated and amino-functionalized structure allows for further chemical modifications, enabling the exploration of diverse biological activities.
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