6-(broMoMethyl)-1-Methylquinazolin-4(1H)-one
97%(HPLC)
- Product Code: 49463
CAS:
1823729-44-7
Molecular Weight: | 253.1 g./mol | Molecular Formula: | C₁₀H₉BrN₂O |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | 391.5±44.0℃(Predicted) | |
Density: | 1.57±0.1 g/cm3(Predicted) | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex quinazoline derivatives. These derivatives are often explored for their potential pharmacological activities, particularly in the development of anticancer and anti-inflammatory agents. The presence of the bromomethyl group makes it a versatile building block, enabling further functionalization through various chemical reactions, such as nucleophilic substitution or coupling reactions. Additionally, it finds application in medicinal chemistry research, where it is used to design and synthesize novel drug candidates targeting specific biological pathways. Its role in the synthesis of heterocyclic compounds also extends to materials science, where such structures are investigated for their electronic and photophysical properties.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.200 | 10-20 days | ฿9,000.00 |
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6-(broMoMethyl)-1-Methylquinazolin-4(1H)-one
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex quinazoline derivatives. These derivatives are often explored for their potential pharmacological activities, particularly in the development of anticancer and anti-inflammatory agents. The presence of the bromomethyl group makes it a versatile building block, enabling further functionalization through various chemical reactions, such as nucleophilic substitution or coupling reactions. Additionally, it finds application in medicinal chemistry research, where it is used to design and synthesize novel drug candidates targeting specific biological pathways. Its role in the synthesis of heterocyclic compounds also extends to materials science, where such structures are investigated for their electronic and photophysical properties.
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