7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinazoline
≥95%
- Product Code: 120949
CAS:
1375108-46-5
Molecular Weight: | 256.11 g./mol | Molecular Formula: | C₁₄H₁₇BN₂O₂ |
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EC Number: | MDL Number: | MFCD18205965 | |
Melting Point: | Boiling Point: | 390.5±15.0°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The boronate ester group in the structure makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of quinazoline derivatives. These derivatives are often explored for their potential biological activities, including anticancer, antiviral, and anti-inflammatory properties. Additionally, it is utilized in materials science for the development of organic electronic materials and polymers. Its stability and reactivity make it a versatile tool in research and industrial applications.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿7,857.00 |
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0.250 | 10-20 days | ฿12,519.00 |
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1.000 | 10-20 days | ฿31,284.00 |
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7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinazoline
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The boronate ester group in the structure makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of quinazoline derivatives. These derivatives are often explored for their potential biological activities, including anticancer, antiviral, and anti-inflammatory properties. Additionally, it is utilized in materials science for the development of organic electronic materials and polymers. Its stability and reactivity make it a versatile tool in research and industrial applications.
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