3-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
95%
- Product Code: 213981
CAS:
1538623-41-4
| Molecular Weight: | 249.11 g./mol | Molecular Formula: | C₁₃H₂₀BNO₃ |
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| EC Number: | MDL Number: | MFCD24449321 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used in Suzuki-Miyaura cross-coupling reactions as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. The boronate ester group enables efficient carbon-carbon bond formation, making it valuable in constructing biaryl compounds for drug development. Commonly applied in the preparation of active pharmaceutical ingredients (APIs) where aniline derivatives are required. Its methoxy and amino groups allow further functionalization, enhancing versatility in multi-step organic synthesis. Preferred in research and industrial settings for high coupling efficiency and stability under standard reaction conditions.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | $132.62 |
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| 1g | 10-20 days | $556.98 |
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| 5g | 10-20 days | $1,856.61 |
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| 250mg | 10-20 days | $238.71 |
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| 10g | 10-20 days | $2,917.53 |
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3-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
Used in Suzuki-Miyaura cross-coupling reactions as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. The boronate ester group enables efficient carbon-carbon bond formation, making it valuable in constructing biaryl compounds for drug development. Commonly applied in the preparation of active pharmaceutical ingredients (APIs) where aniline derivatives are required. Its methoxy and amino groups allow further functionalization, enhancing versatility in multi-step organic synthesis. Preferred in research and industrial settings for high coupling efficiency and stability under standard reaction conditions.
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