4-Butoxyphenylboronic acid
98%
- Product Code: 90580
Alias:
4-n-butoxyphenylboronic acid
CAS:
105365-51-3
| Molecular Weight: | 194.04 g./mol | Molecular Formula: | C₁₀H₁₅BO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03427054 | |
| Melting Point: | 106-108 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
4-Butoxyphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling of aryl or vinyl halides with aryl or vinyl boronic acids. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with diols and sugars, making it useful in glucose sensing and other biochemical applications. Its stability and reactivity make it a valuable compound in both industrial and research settings.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 106-108 |
| PurityGC | 98-100 |
| APPEARANCE | White to off-white powder |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿280.00 |
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| 1.000 | 10-20 days | ฿960.00 |
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| 5.000 | 10-20 days | ฿2,780.00 |
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| 25.000 | 10-20 days | ฿12,260.00 |
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4-Butoxyphenylboronic acid
4-Butoxyphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling of aryl or vinyl halides with aryl or vinyl boronic acids. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with diols and sugars, making it useful in glucose sensing and other biochemical applications. Its stability and reactivity make it a valuable compound in both industrial and research settings.
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