Tert-butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate
98%
- Product Code: 83521
CAS:
942070-47-5
| Molecular Weight: | 344.21 g./mol | Molecular Formula: | C₁₈H₂₅BN₂O₄ |
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| EC Number: | MDL Number: | MFCD12407268 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, store under inert gas |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in the pharmaceutical industry where it aids in the development of drug candidates. The tert-butyl carbamate protecting group ensures stability during reactions, allowing for selective modifications. It is also employed in the synthesis of heterocyclic compounds, which are crucial in creating biologically active molecules for medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft21,817.57 |
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| 0.250 | 10-20 days | Ft36,750.48 |
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| 1.000 | 10-20 days | Ft73,694.90 |
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Tert-butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in the pharmaceutical industry where it aids in the development of drug candidates. The tert-butyl carbamate protecting group ensures stability during reactions, allowing for selective modifications. It is also employed in the synthesis of heterocyclic compounds, which are crucial in creating biologically active molecules for medicinal chemistry research.
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