4-Methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
≥97%
- Product Code: 210594
CAS:
948592-80-1
| Molecular Weight: | 233.11 g./mol | Molecular Formula: | C₁₃H₂₀BNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06795664 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, avoid light, inert gas storage |
Product Description:
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds with aryl or heteroaryl halides. This makes it valuable in drug discovery and development of functional materials. It is also employed in the preparation of conjugated organic molecules for use in optoelectronics and advanced polymers. The presence of the aniline moiety offers a site for further functionalization, increasing its versatility in multi-step synthetic routes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿2,930.00 |
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| 1g | 10-20 days | ฿5,920.00 |
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| 5g | 10-20 days | ฿21,290.00 |
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| 25g | 10-20 days | ฿104,620.00 |
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4-Methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds with aryl or heteroaryl halides. This makes it valuable in drug discovery and development of functional materials. It is also employed in the preparation of conjugated organic molecules for use in optoelectronics and advanced polymers. The presence of the aniline moiety offers a site for further functionalization, increasing its versatility in multi-step synthetic routes.
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