(4-Octylphenyl)boronic acid
97%
- Product Code: 113331
CAS:
133997-05-4
| Molecular Weight: | 234.14 g./mol | Molecular Formula: | C₁₄H₂₃BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04039034 | |
| Melting Point: | Boiling Point: | 371.2°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
(4-Octylphenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key reagent, enabling the coupling of aryl or vinyl boronic acids with aryl or vinyl halides in the presence of a palladium catalyst. Its octyl chain enhances solubility in organic solvents, facilitating efficient reaction conditions. Additionally, it finds applications in the development of sensors and as a building block in the synthesis of complex organic molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,907.00 |
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| 0.250 | 10-20 days | ฿5,814.00 |
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(4-Octylphenyl)boronic acid
(4-Octylphenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key reagent, enabling the coupling of aryl or vinyl boronic acids with aryl or vinyl halides in the presence of a palladium catalyst. Its octyl chain enhances solubility in organic solvents, facilitating efficient reaction conditions. Additionally, it finds applications in the development of sensors and as a building block in the synthesis of complex organic molecules.
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