2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)isoindoline-1,3-dione
95%
- Product Code: 242208
Alias:
4-phthaliminomethylphenylborate
CAS:
138500-87-5
| Molecular Weight: | 363.22 g./mol | Molecular Formula: | C₂₁H₂₂BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02179489 | |
| Melting Point: | Boiling Point: | 504°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key boronic ester precursor. Its primary application lies in the construction of biaryl and aryl-heteroaryl frameworks, which are common structural motifs in pharmaceuticals, agrochemicals, and functional materials. The presence of the isoindoline-1,3-dione group enhances stability and can act as a protecting group or directing handle in multi-step syntheses. It is especially valuable in drug discovery and development for enabling efficient carbon-carbon bond formation under mild conditions.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,270.00 |
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| 5.000 | 10-20 days | ฿6,310.00 |
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| 25.000 | 10-20 days | ฿22,700.00 |
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2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)isoindoline-1,3-dione
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key boronic ester precursor. Its primary application lies in the construction of biaryl and aryl-heteroaryl frameworks, which are common structural motifs in pharmaceuticals, agrochemicals, and functional materials. The presence of the isoindoline-1,3-dione group enhances stability and can act as a protecting group or directing handle in multi-step syntheses. It is especially valuable in drug discovery and development for enabling efficient carbon-carbon bond formation under mild conditions.
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