2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
97%
- Product Code: 116856
CAS:
590418-05-6
| Molecular Weight: | 233.11 g./mol | Molecular Formula: | C₁₃H₂₀BNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09033882 | |
| Melting Point: | Boiling Point: | 359.0±35.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester group acts as a key intermediate, enabling the introduction of aromatic amines into complex molecules. Additionally, it is employed in the development of organic light-emitting diodes (OLEDs) and other electronic materials due to its ability to modify electronic properties. Its stability and reactivity make it a preferred choice in research and industrial applications for creating diverse organic compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿900.00 |
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| 0.250 | 10-20 days | ฿1,764.00 |
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| 1.000 | 10-20 days | ฿3,420.00 |
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2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester group acts as a key intermediate, enabling the introduction of aromatic amines into complex molecules. Additionally, it is employed in the development of organic light-emitting diodes (OLEDs) and other electronic materials due to its ability to modify electronic properties. Its stability and reactivity make it a preferred choice in research and industrial applications for creating diverse organic compounds.
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