4-(Dibenzylaminomethyl) phenylboronic acid
95%
- Product Code: 46473
CAS:
1221824-11-8
Molecular Weight: | 331.21588 g./mol | Molecular Formula: | C₂₁H₂₂BNO₂ |
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Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex boronic acid derivatives. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the synthesis of pharmaceuticals, agrochemicals, and organic materials. The dibenzylaminomethyl group enhances the stability and reactivity of the boronic acid, making it suitable for constructing carbon-carbon bonds in the presence of palladium catalysts. Additionally, it finds application in the development of sensors and probes for detecting sugars and other diol-containing molecules, leveraging its boronic acid moiety’s affinity for such compounds. Its versatility also extends to the field of polymer chemistry, where it is used to modify polymer chains for specific functional properties.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿14,508.00 |
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0.250 | 10-20 days | ฿24,192.00 |
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1.000 | 10-20 days | ฿64,512.00 |
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4-(Dibenzylaminomethyl) phenylboronic acid
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex boronic acid derivatives. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the synthesis of pharmaceuticals, agrochemicals, and organic materials. The dibenzylaminomethyl group enhances the stability and reactivity of the boronic acid, making it suitable for constructing carbon-carbon bonds in the presence of palladium catalysts. Additionally, it finds application in the development of sensors and probes for detecting sugars and other diol-containing molecules, leveraging its boronic acid moiety’s affinity for such compounds. Its versatility also extends to the field of polymer chemistry, where it is used to modify polymer chains for specific functional properties.
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