2-(3,4-Dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
3,4-Dimethylphenylboronic acid pinacol ester
CAS: 401797-00-0
Molecular Formula: C14H21BO2
2-(3,4-Dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane - Names and Identifiers
2-(3,4-Dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane - Physico-chemical Properties
| Molecular Formula | C14H21BO2 |
| Molar Mass | 232.13 |
| Density | 0.97±0.1 g/cm3(Predicted) |
| Melting Point | 35 °C |
| Boling Point | 325.4±31.0 °C(Predicted) |
| Appearance | powder to lump |
| Color | White to Almost white |
| Storage Condition | Inert atmosphere,2-8°C |
| Sensitive | Irritant |
| MDL | MFCD12405519 |
2-(3,4-Dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane - Introduction
3,4-Dimethylphenylboronic acid pinacol ester is an organic compound whose chemical formula is C14H21BO3. It is a solid, colorless or pale yellow crystal.
3,4-Dimethylphenylboronic acid pinacol ester is an important organic boron compound, which is widely used in the field of organic synthesis. It can be used as a substrate and reagent to participate in the functional group conversion and coupling reaction of phenyl. For example, it can be used in the synthesis of enantiomeric fullerenyl heterocyclic compounds, the preparation of a variety of biologically active peptide compounds, and the synthesis of flavors and pharmaceutical intermediates.
The method for preparing 3,4-Dimethylphenylboronic acid pinacol ester is usually to react 3,4-dimethylbenzeneboronic acid with pineol. Specifically, 3,4-dimethylphenylboronic acid and pone alcohol are reacted in an appropriate solvent, and a catalyst is added, and the product is obtained after an appropriate temperature and time.
Regarding safety information, 3,4-Dimethylboronic acid pinacol ester should refer to relevant chemical safety manuals or chemical-related databases for specific safety information. When using and handling the compound, appropriate laboratory practices should be followed, appropriate protective equipment should be worn, and proper chemical waste disposal procedures should be followed.
3,4-Dimethylphenylboronic acid pinacol ester is an important organic boron compound, which is widely used in the field of organic synthesis. It can be used as a substrate and reagent to participate in the functional group conversion and coupling reaction of phenyl. For example, it can be used in the synthesis of enantiomeric fullerenyl heterocyclic compounds, the preparation of a variety of biologically active peptide compounds, and the synthesis of flavors and pharmaceutical intermediates.
The method for preparing 3,4-Dimethylphenylboronic acid pinacol ester is usually to react 3,4-dimethylbenzeneboronic acid with pineol. Specifically, 3,4-dimethylphenylboronic acid and pone alcohol are reacted in an appropriate solvent, and a catalyst is added, and the product is obtained after an appropriate temperature and time.
Regarding safety information, 3,4-Dimethylboronic acid pinacol ester should refer to relevant chemical safety manuals or chemical-related databases for specific safety information. When using and handling the compound, appropriate laboratory practices should be followed, appropriate protective equipment should be worn, and proper chemical waste disposal procedures should be followed.
Last Update：2024-04-09 20:02:46
