(E)-n-Tert-butyl-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanimine
4-(t-Butyl)iminomethyl phenyl-boronic acid pinacol ester
CAS: 1218790-47-6
Molecular Formula: C17H26BNO2
(E)-n-Tert-butyl-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanimine - Names and Identifiers
(E)-n-Tert-butyl-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanimine - Physico-chemical Properties
| Molecular Formula | C17H26BNO2 |
| Molar Mass | 287.2 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD11113039 |
(E)-n-Tert-butyl-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanimine - Introduction
4-(t-Butyl)iminomethyl phenyl-boronic acid pinacol ester(4-(t-Butyl)iminomethyl phenyl-boronic acid pinacol ester), also known as 4-(tert-butyl) methylenebenzeneboronic acid propanediol ester, is an organic compound.
Properties: This compound is a solid, the structure contains methylene benzene boronic acid group and tert-butyl group, with high solubility. It is an important boric acid reagent with certain stability.
use: 4-(t-Butyl)iminomethyl phenyl-boronic acid pinacol ester is widely used in organic synthesis. It can be used as a boronic acid reagent to participate in coupling reactions, Schweizi reactions and other important organic synthesis reactions. In addition, it can also be used to prepare complexes and catalysts.
preparation method: 4-(t-Butyl)iminomethyl phenyl-boronic acid pinacol ester preparation method is more complex, usually need to use organic synthesis technology. A common method of preparation is to react methylenebenzeneboronic acid with tert-butylamine followed by reaction with propal to obtain the product.
Safety information: Because 4-(t-Butyl)iminomethyl phenyl-boronic acid pinacol ester does not have extensive toxicity studies, evaluation of its safety is relatively limited. However, care should be taken to avoid contact with skin and eyes and maintain good ventilation. At the same time, the preparation and handling of the compound need to comply with the appropriate laboratory safety procedures.
Properties: This compound is a solid, the structure contains methylene benzene boronic acid group and tert-butyl group, with high solubility. It is an important boric acid reagent with certain stability.
use: 4-(t-Butyl)iminomethyl phenyl-boronic acid pinacol ester is widely used in organic synthesis. It can be used as a boronic acid reagent to participate in coupling reactions, Schweizi reactions and other important organic synthesis reactions. In addition, it can also be used to prepare complexes and catalysts.
preparation method: 4-(t-Butyl)iminomethyl phenyl-boronic acid pinacol ester preparation method is more complex, usually need to use organic synthesis technology. A common method of preparation is to react methylenebenzeneboronic acid with tert-butylamine followed by reaction with propal to obtain the product.
Safety information: Because 4-(t-Butyl)iminomethyl phenyl-boronic acid pinacol ester does not have extensive toxicity studies, evaluation of its safety is relatively limited. However, care should be taken to avoid contact with skin and eyes and maintain good ventilation. At the same time, the preparation and handling of the compound need to comply with the appropriate laboratory safety procedures.
Last Update：2024-04-09 21:11:58
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