2-(2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethyl)isoindoline-1,3-dione
96%
- Product Code: 243618
CAS:
957061-09-5
| Molecular Weight: | 393.2 g./mol | Molecular Formula: | C₂₂H₂₄BNO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09258656 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the preparation of complex organic molecules, including pharmaceuticals and functional materials. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development. Its phthalimide moiety can be deprotected to release amines, allowing further functionalization in multi-step syntheses. Commonly employed in the construction of biaryl systems, it supports the creation of advanced intermediates for agrochemicals, OLED materials, and bioactive compounds.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿4,330.00 |
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| 100mg | 10-20 days | ฿2,190.00 |
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2-(2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethyl)isoindoline-1,3-dione
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the preparation of complex organic molecules, including pharmaceuticals and functional materials. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development. Its phthalimide moiety can be deprotected to release amines, allowing further functionalization in multi-step syntheses. Commonly employed in the construction of biaryl systems, it supports the creation of advanced intermediates for agrochemicals, OLED materials, and bioactive compounds.
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