o-Tolylboronic acid
98%
- Product Code: 89838
Alias:
2-Methylphenylboronic acid
CAS:
16419-60-6
| Molecular Weight: | 135.96 g./mol | Molecular Formula: | C₇H₉BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00093526 | |
| Melting Point: | 162-164 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
o-Tolylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. It serves as a key reagent in the production of biaryl compounds, which are common structural motifs in many drugs and functional materials. Additionally, it is employed in the development of organic electronic materials, such as OLEDs, due to its ability to introduce aromatic groups into molecular frameworks. Its stability and reactivity make it a valuable tool in medicinal chemistry for creating diverse chemical libraries for drug discovery.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97.5 100% |
| APPEARANCE | White to Off White Solid to Crystals to Flakes to Crystalline Powder to Powder |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 1.000 | 10-20 days | $12.68 |
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| 5.000 | 10-20 days | $16.91 |
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| 25.000 | 10-20 days | $49.78 |
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| 100.000 | 10-20 days | $181.75 |
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| 500.000 | 10-20 days | $874.00 |
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o-Tolylboronic acid
o-Tolylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. It serves as a key reagent in the production of biaryl compounds, which are common structural motifs in many drugs and functional materials. Additionally, it is employed in the development of organic electronic materials, such as OLEDs, due to its ability to introduce aromatic groups into molecular frameworks. Its stability and reactivity make it a valuable tool in medicinal chemistry for creating diverse chemical libraries for drug discovery.
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