1-Methyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine
95%
- Product Code: 209679
CAS:
1644629-23-1
| Molecular Weight: | 258.12 g./mol | Molecular Formula: | C₁₄H₁₉BN₂O₂ |
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| EC Number: | MDL Number: | MFCD17214359 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, airtight, dry |
Product Description:
Used in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions to construct biaryl or heteroaryl frameworks. Its pyrrolopyridine core makes it valuable in pharmaceutical and agrochemical research for building complex nitrogen-containing heterocycles. The tetramethyl dioxaborolane group provides stability and reactivity under palladium catalysis, enabling efficient carbon-carbon bond formation. Commonly employed in late-stage functionalization of bioactive molecules and in the development of kinase inhibitors and other therapeutic agents.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿929.50 |
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| 1g | 10-20 days | ฿4,490.00 |
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| 25g | 10-20 days | ฿81,350.00 |
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| 5g | 10-20 days | ฿16,960.00 |
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1-Methyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine
Used in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions to construct biaryl or heteroaryl frameworks. Its pyrrolopyridine core makes it valuable in pharmaceutical and agrochemical research for building complex nitrogen-containing heterocycles. The tetramethyl dioxaborolane group provides stability and reactivity under palladium catalysis, enabling efficient carbon-carbon bond formation. Commonly employed in late-stage functionalization of bioactive molecules and in the development of kinase inhibitors and other therapeutic agents.
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