2-(3-Methoxypropoxy)phenylboronic acid
98%
- Product Code: 89624
CAS:
1122568-12-0
| Molecular Weight: | 210.04 g./mol | Molecular Formula: | C₁₀H₁₅BO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12768318 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the creation of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it is utilized in material science for synthesizing advanced polymers and organic electronic materials. Its methoxypropoxy group enhances solubility and stability, making it suitable for various reaction conditions. This compound is also employed in the development of sensors and probes for detecting specific biological molecules due to its selective binding properties.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | $1,194.22 |
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2-(3-Methoxypropoxy)phenylboronic acid
This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the creation of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it is utilized in material science for synthesizing advanced polymers and organic electronic materials. Its methoxypropoxy group enhances solubility and stability, making it suitable for various reaction conditions. This compound is also employed in the development of sensors and probes for detecting specific biological molecules due to its selective binding properties.
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