(1-Methyl-1H-benzo[d]imidazol-5-yl)boronic acid
≥98%
- Product Code: 192496
CAS:
1107627-21-3
| Molecular Weight: | 175.98 g./mol | Molecular Formula: | C₈H₉BN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16036273 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, Sealed, Inert Gas |
Product Description:
Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct biaryl compounds which are common scaffolds in pharmaceuticals and agrochemicals. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in drug discovery for building nitrogen-containing heterocyclic systems. Also utilized in the development of fluorescent probes and functional materials due to the benzimidazole core’s photophysical properties. Stable enough for handling in air, making it practical for laboratory-scale synthesis.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 G | 10-20 days | ฿6,340.00 |
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| 0.500 G | 10-20 days | ฿11,860.00 |
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| 1.000 G | 10-20 days | ฿16,920.00 |
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| 0.100 G | 10-20 days | ฿3,700.00 |
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(1-Methyl-1H-benzo[d]imidazol-5-yl)boronic acid
Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct biaryl compounds which are common scaffolds in pharmaceuticals and agrochemicals. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in drug discovery for building nitrogen-containing heterocyclic systems. Also utilized in the development of fluorescent probes and functional materials due to the benzimidazole core’s photophysical properties. Stable enough for handling in air, making it practical for laboratory-scale synthesis.
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