4-Aminophenylboronic acid pinacol ester
98%
- Product Code: 90619
Alias:
4-Aminophenylboronic acid pinacol ester
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
CAS:
214360-73-3
Molecular Weight: | 219.09 g./mol | Molecular Formula: | C₁₂H₁₈BNO₂ |
---|---|---|---|
EC Number: | MDL Number: | MFCD02093721 | |
Melting Point: | 165-169 °C(lit.) | Boiling Point: | |
Density: | Storage Condition: | 2~8°C |
Product Description:
Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds. These compounds are essential in pharmaceuticals, agrochemicals, and materials science. It also serves as a building block for designing sensors and probes due to its boronic acid group, which can selectively bind to diols and sugars. Applied in the development of glucose-sensitive devices for diabetes management. Additionally, it plays a role in the preparation of advanced polymers and functionalized materials.
Product Specification:
Test | Specification |
---|---|
CARBON | 63.5-68.1 |
Melting point | 166-170 |
NITROGEN | 6.1-6.6 |
Purity | 98-100 |
APPEARANCE | WHITE TO BROWN CRYSTALS OR POWDER CHUNKS |
INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿360.00 |
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5.000 | 10-20 days | ฿1,060.00 |
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25.000 | 10-20 days | ฿4,350.00 |
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4-Aminophenylboronic acid pinacol ester
Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds. These compounds are essential in pharmaceuticals, agrochemicals, and materials science. It also serves as a building block for designing sensors and probes due to its boronic acid group, which can selectively bind to diols and sugars. Applied in the development of glucose-sensitive devices for diabetes management. Additionally, it plays a role in the preparation of advanced polymers and functionalized materials.
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