4-(Diphenylamino)phenylboronic acid
98%
- Product Code: 90538
Alias:
4-(Diphenylamino)phenylboronic acid Triphenylamine-4-boronic acid
CAS:
201802-67-7
| Molecular Weight: | 289.14 g./mol | Molecular Formula: | C₁₈H₁₆BNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06798117 | |
| Melting Point: | 110-115 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of complex organic molecules, including pharmaceuticals and advanced materials. Additionally, it serves as a building block in the development of organic electronic materials, such as organic light-emitting diodes (OLEDs) and organic photovoltaic cells, due to its electron-donating diphenylamino group. Its unique structure also makes it useful in sensor applications, where it can detect specific analytes through boronic acid-diol interactions.
Product Specification:
| Test | Specification |
|---|---|
| PURITYNEUTRALIZATION TITRATION | 97.5-102.5 |
| APPEARANCE | White to off-white powder,crystals and/or chunks |
| INFRARED SPECTRUM | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿410.00 |
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| 5.000 | 10-20 days | ฿1,400.00 |
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| 25.000 | 10-20 days | ฿6,380.00 |
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| 100.000 | 10-20 days | ฿22,880.00 |
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4-(Diphenylamino)phenylboronic acid
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of complex organic molecules, including pharmaceuticals and advanced materials. Additionally, it serves as a building block in the development of organic electronic materials, such as organic light-emitting diodes (OLEDs) and organic photovoltaic cells, due to its electron-donating diphenylamino group. Its unique structure also makes it useful in sensor applications, where it can detect specific analytes through boronic acid-diol interactions.
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