tert-butyl 8-methyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine-1-carboxylate
95%
- Product Code: 60430
CAS:
2246363-82-4
| Molecular Weight: | 376.2538 g./mol | Molecular Formula: | C₁₉H₂₉BN₂O₅ |
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| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester group enables efficient participation in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic molecules, such as pharmaceuticals and agrochemicals. The tert-butyloxycarbonyl (Boc) protecting group enhances its stability during reactions, making it suitable for multi-step synthetic processes. Its application is especially valuable in the development of biologically active compounds, where precise structural modifications are required.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿10,224.00 |
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| 0.500 | 10-20 days | ฿35,766.00 |
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tert-butyl 8-methyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine-1-carboxylate
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester group enables efficient participation in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic molecules, such as pharmaceuticals and agrochemicals. The tert-butyloxycarbonyl (Boc) protecting group enhances its stability during reactions, making it suitable for multi-step synthetic processes. Its application is especially valuable in the development of biologically active compounds, where precise structural modifications are required.
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