2-MEthoxy-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
95%
- Product Code: 43565
CAS:
1609393-90-9
| Molecular Weight: | 249.1138 g./mol | Molecular Formula: | C₁₃H₂₀BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27936703 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group enables efficient formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of heterocyclic compounds, which are essential in drug discovery and material science. The methoxy and aniline groups further enhance its reactivity and selectivity in various chemical transformations, contributing to its versatility in synthetic chemistry applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $300.14 |
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2-MEthoxy-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group enables efficient formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of heterocyclic compounds, which are essential in drug discovery and material science. The methoxy and aniline groups further enhance its reactivity and selectivity in various chemical transformations, contributing to its versatility in synthetic chemistry applications.
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