2-(3-Isopropylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
98%
- Product Code: 200162
CAS:
325142-89-0
| Molecular Weight: | 246.1600 g./mol | Molecular Formula: | C₁₅H₂₃BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13195750 | |
| Melting Point: | Boiling Point: | 326.0±21.0℃(Predicted) | |
| Density: | 0.96±0.1g/ml(Predicted) | Storage Condition: | 2-8℃, dry, sealed |
Product Description:
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. It serves as a stable boronic ester derivative, facilitating the preparation of biaryl compounds widely found in pharmaceuticals, agrochemicals, and advanced materials. Its isopropyl-substituted phenyl group allows for selective coupling in complex molecule assembly, making it valuable in drug discovery and development processes. The compound’s stability and reactivity profile support efficient transformations under mild conditions, particularly in late-stage functionalization of bioactive molecules.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | Ft24,157.48 |
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| 5g | 10-20 days | Ft97,039.36 |
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2-(3-Isopropylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. It serves as a stable boronic ester derivative, facilitating the preparation of biaryl compounds widely found in pharmaceuticals, agrochemicals, and advanced materials. Its isopropyl-substituted phenyl group allows for selective coupling in complex molecule assembly, making it valuable in drug discovery and development processes. The compound’s stability and reactivity profile support efficient transformations under mild conditions, particularly in late-stage functionalization of bioactive molecules.
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