4-Chloro-6,7-difluoro-2-methylquinazoline
95%
- Product Code: 47177
CAS:
887592-02-1
Molecular Weight: | 214.5992 g./mol | Molecular Formula: | C₉H₅ClF₂N₂ |
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EC Number: | MDL Number: | MFCD06657231 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
4-Chloro-6,7-difluoro-2-methylquinazoline 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 kinase inhibitors, which are essential in targeted cancer therapies. The compound’s quinazoline core allows for modifications that enhance binding affinity and selectivity toward specific enzyme targets, making it a critical building block in drug discovery. Additionally, it is employed in the preparation of compounds with potential antiviral and antibacterial properties, contributing to the development of new treatments for infectious diseases. Its versatility in organic synthesis also extends to the creation of fluorescent probes and other research tools used in biochemical studies.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.050 | 10-20 days | ฿1,926.00 |
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4-Chloro-6,7-difluoro-2-methylquinazoline
4-Chloro-6,7-difluoro-2-methylquinazoline 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 kinase inhibitors, which are essential in targeted cancer therapies. The compound’s quinazoline core allows for modifications that enhance binding affinity and selectivity toward specific enzyme targets, making it a critical building block in drug discovery. Additionally, it is employed in the preparation of compounds with potential antiviral and antibacterial properties, contributing to the development of new treatments for infectious diseases. Its versatility in organic synthesis also extends to the creation of fluorescent probes and other research tools used in biochemical studies.
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