6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,2,4]triazolo[4,3-a]pyridine
97%
- Product Code: 241720
CAS:
1314137-24-0
| Molecular Weight: | 245.09 g./mol | Molecular Formula: | C₁₂H₁₆BN₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26403534 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, stored in inert gas |
Product Description:
Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in medicinal chemistry for constructing biaryl and heteroaryl frameworks. It is particularly useful in the development of kinase inhibitors and other bioactive molecules where the triazolopyridine scaffold enhances binding affinity and metabolic stability. The reagent’s compatibility with diverse functional groups allows for late-stage functionalization in complex molecule synthesis, streamlining drug discovery and optimization processes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿3,760.00 |
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| 250mg | 10-20 days | ฿6,150.00 |
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| 1g | 10-20 days | ฿12,830.00 |
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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,2,4]triazolo[4,3-a]pyridine
Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in medicinal chemistry for constructing biaryl and heteroaryl frameworks. It is particularly useful in the development of kinase inhibitors and other bioactive molecules where the triazolopyridine scaffold enhances binding affinity and metabolic stability. The reagent’s compatibility with diverse functional groups allows for late-stage functionalization in complex molecule synthesis, streamlining drug discovery and optimization processes.
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