Ethyl 3-amino-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
98%
- Product Code: 184983
CAS:
1350989-93-3
| Molecular Weight: | 291.15 g./mol | Molecular Formula: | C₁₅H₂₂BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22192537 | |
| Melting Point: | Boiling Point: | 425.5±35.0 °C(Predicted) | |
| Density: | 1.11±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, light-proof |
Product Description:
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex aromatic compounds in pharmaceutical and agrochemical development. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions. Commonly employed in the preparation of biaryl structures found in active pharmaceutical ingredients. Also utilized in materials science for constructing conjugated systems in organic electronics. The presence of both amino and ester functionalities allows for further selective derivatization, enhancing its versatility in multi-step syntheses.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 G | 10-20 days | ฿750.00 |
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| 0.250 G | 10-20 days | ฿1,630.00 |
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Ethyl 3-amino-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex aromatic compounds in pharmaceutical and agrochemical development. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions. Commonly employed in the preparation of biaryl structures found in active pharmaceutical ingredients. Also utilized in materials science for constructing conjugated systems in organic electronics. The presence of both amino and ester functionalities allows for further selective derivatization, enhancing its versatility in multi-step syntheses.
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