(4-(2-Aminoethyl)phenyl)boronic acid
98%
- Product Code: 131876
CAS:
68162-46-9
| Molecular Weight: | 165 g./mol | Molecular Formula: | C₈H₁₂BNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06212996 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, light-proof, inert gas |
Product Description:
Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to construct biaryl compounds, which are common scaffolds in pharmaceuticals and agrochemicals. Its amine and boronic acid functional groups allow for dual reactivity, enabling conjugation in bioconjugation chemistry and the development of sensors for detecting carbohydrates or saccharides. Also serves as a building block in drug discovery for creating enzyme inhibitors or targeted therapeutics. Its structure supports solid-phase synthesis and immobilization on surfaces for diagnostic applications.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,910.00 |
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| 0.250 | 10-20 days | ฿10,040.00 |
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| 1.000 | 10-20 days | ฿26,060.00 |
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| 5.000 | 10-20 days | ฿87,500.00 |
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| 10.000 | 10-20 days | ฿159,250.00 |
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(4-(2-Aminoethyl)phenyl)boronic acid
Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to construct biaryl compounds, which are common scaffolds in pharmaceuticals and agrochemicals. Its amine and boronic acid functional groups allow for dual reactivity, enabling conjugation in bioconjugation chemistry and the development of sensors for detecting carbohydrates or saccharides. Also serves as a building block in drug discovery for creating enzyme inhibitors or targeted therapeutics. Its structure supports solid-phase synthesis and immobilization on surfaces for diagnostic applications.
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