2-(6-(tert-butyl)-8-fluoro-1-oxophthalazin-2(1H)-yl)-6-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzyl acetate
- Product Code: 77082
CAS:
1242156-76-8
| Molecular Weight: | 494.36 g./mol | Molecular Formula: | C₂₇H₃₂BFN₂O₅ |
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| EC Number: | MDL Number: | MFCD26403976 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronic ester functional group makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in complex molecules. The presence of the phthalazine moiety enhances its potential as a building block for biologically active compounds, including inhibitors and modulators of specific enzymes or receptors. Additionally, the tert-butyl and fluorine substituents contribute to its stability and selectivity in various chemical transformations, making it a versatile reagent in medicinal chemistry research. Its application extends to the synthesis of novel drug candidates targeting diseases such as cancer, inflammation, and infectious diseases.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿545,904.00 |
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2-(6-(tert-butyl)-8-fluoro-1-oxophthalazin-2(1H)-yl)-6-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzyl acetate
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronic ester functional group makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in complex molecules. The presence of the phthalazine moiety enhances its potential as a building block for biologically active compounds, including inhibitors and modulators of specific enzymes or receptors. Additionally, the tert-butyl and fluorine substituents contribute to its stability and selectivity in various chemical transformations, making it a versatile reagent in medicinal chemistry research. Its application extends to the synthesis of novel drug candidates targeting diseases such as cancer, inflammation, and infectious diseases.
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