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2-Indanylboronic acid pinacol ester, 95%, Thermo Scientific Chemicals
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Quantity:
250 mg
1 g
Description
Boronic acids react with alcohols, with loss of water, to form boronic esters. With simple alcohols, the products are very susceptible to hydrolysis, but with 1,2- and 1,3-diols, the resulting cyclic boronates (1,3,2- dioxaborolanes and 1,3,2-dioxaborinanes) are stable enough to be isolated.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Boronic acids react with alcohols, with loss of water, to form boronic esters. With simple alcohols, the products are very susceptible to hydrolysis, but with 1,2- and 1,3-diols, the resulting cyclic boronates (1,3,2- dioxaborolanes and 1,3,2-dioxaborinanes) are stable enough to be isolated.
Solubility
Difficult to mix in water.
Notes
Store at room temperature. Incompatible with oxidizing agents.
Boronic acids react with alcohols, with loss of water, to form boronic esters. With simple alcohols, the products are very susceptible to hydrolysis, but with 1,2- and 1,3-diols, the resulting cyclic boronates (1,3,2- dioxaborolanes and 1,3,2-dioxaborinanes) are stable enough to be isolated.
Solubility
Difficult to mix in water.
Notes
Store at room temperature. Incompatible with oxidizing agents.
Specifications
Specifications
| Refractive Index | 1.504 |
| Quantity | 250 mg |
| Solubility Information | Difficult to mix in water. |
| Formula Weight | 244.14 |
| Percent Purity | 95% |
| Chemical Name or Material | 2-Indanylboronic acid pinacol ester |
RUO – Research Use Only
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