sec-Butylboronic acid
95%
- Product Code: 91101
Alias:
sec-butylboronic acid
2-Butylboronic acid
CAS:
88496-88-2
| Molecular Weight: | 101.94 g./mol | Molecular Formula: | C₄H₁₁BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06656265 | |
| Melting Point: | 85-89 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
sec-Butylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate in the synthesis of complex organic molecules, enabling the introduction of the sec-butyl group into target structures. It is also employed in the development of boron-containing compounds, which have applications in medicinal chemistry and drug discovery. Additionally, sec-butylboronic acid is utilized in research for studying reaction mechanisms and developing new catalytic processes. Its stability and reactivity make it a versatile reagent in various chemical transformations.
Product Specification:
| Test | Specification |
|---|---|
| PURITYTITRATION WITH NAOH | 95-105 |
| APPEARANCE | White to yellow solid |
| INFRARED SPECTRUM | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿560.00 |
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| 5.000 | 10-20 days | ฿2,280.00 |
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| 25.000 | 10-20 days | ฿10,680.00 |
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sec-Butylboronic acid
sec-Butylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate in the synthesis of complex organic molecules, enabling the introduction of the sec-butyl group into target structures. It is also employed in the development of boron-containing compounds, which have applications in medicinal chemistry and drug discovery. Additionally, sec-butylboronic acid is utilized in research for studying reaction mechanisms and developing new catalytic processes. Its stability and reactivity make it a versatile reagent in various chemical transformations.
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