3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
98%
- Product Code: 208579
CAS:
1073354-66-1
| Molecular Weight: | 246.11 g./mol | Molecular Formula: | C₁₄H₁₉BO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08669583 | |
| Melting Point: | Boiling Point: | 358.7±35.0℃ at 760 mmHg | |
| Density: | 1.05±0.1 g/cm3 | Storage Condition: | 2-8℃, sealed, dried |
Product Description:
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its aldehyde and boronate functional groups allow dual reactivity, enabling sequential transformations to build aromatic frameworks. Commonly employed in the development of conjugated materials for optoelectronics and in medicinal chemistry to construct biaryl aldehyde derivatives with biological activity. The boronate ester group facilitates mild, selective coupling with aryl halides, making it valuable in late-stage functionalization during drug discovery.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿2,890.00 |
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| 250mg | 10-20 days | ฿4,710.00 |
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| 1g | 10-20 days | ฿12,960.00 |
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3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its aldehyde and boronate functional groups allow dual reactivity, enabling sequential transformations to build aromatic frameworks. Commonly employed in the development of conjugated materials for optoelectronics and in medicinal chemistry to construct biaryl aldehyde derivatives with biological activity. The boronate ester group facilitates mild, selective coupling with aryl halides, making it valuable in late-stage functionalization during drug discovery.
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