1073353-60-2
[4-(2-Methoxyethylamine-1-carbonyl)-phenyl]boronic acid pinacol ester
CAS: 1073353-60-2
Molecular Formula: C16H24BNO4
1073353-60-2 - Names and Identifiers
1073353-60-2 - Physico-chemical Properties
| Molecular Formula | C16H24BNO4 |
| Molar Mass | 305.18 |
| Melting Point | 73-76°C |
| Storage Condition | 2-8°C |
| Sensitive | Irritant |
| MDL | MFCD09266188 |
1073353-60-2 - Introduction
[4-(5)-phenyl]boronic acid pinacol ester, or MEAC-Bpin for short, is an organic compound. Its chemical formula is C16H23BO4N and its molecular weight is 301.17g/mol.
Nature:
MEAC-Bpin is a white to light yellow solid with good solubility. It is an organic borate ester that can form stable complexes with good air and humidity stability.
Use:
MEAC-Bpin can be used as a reagent for organic synthesis. It can react with other compounds to form complexes for catalytic reduction reactions, coupling reactions and other organic synthesis reactions. In addition, MEAC-Bpin can also be used in the fields of drug research and development and the synthesis of hybrid materials.
Preparation Method:
The preparation method of MEAC-Bpin is mainly realized by chemical synthesis. A common synthetic method is the reduction of the amino oxyethyl group to an amine group in the presence of a base by a nucleophilic substitution reaction and reaction with a phenyl borate to yield the target product.
Safety Information:
Although MEAC-Bpin is a relatively safe compound, as an organic chemical reagent, it is still necessary to pay attention to safe use. Avoid direct contact with skin, eyes and inhalation during operation. The working environment requires good ventilation and the use of personal protective equipment, such as laboratory gloves, eye protection, etc. If swallowed or taken by mistake, seek medical attention immediately.
Nature:
MEAC-Bpin is a white to light yellow solid with good solubility. It is an organic borate ester that can form stable complexes with good air and humidity stability.
Use:
MEAC-Bpin can be used as a reagent for organic synthesis. It can react with other compounds to form complexes for catalytic reduction reactions, coupling reactions and other organic synthesis reactions. In addition, MEAC-Bpin can also be used in the fields of drug research and development and the synthesis of hybrid materials.
Preparation Method:
The preparation method of MEAC-Bpin is mainly realized by chemical synthesis. A common synthetic method is the reduction of the amino oxyethyl group to an amine group in the presence of a base by a nucleophilic substitution reaction and reaction with a phenyl borate to yield the target product.
Safety Information:
Although MEAC-Bpin is a relatively safe compound, as an organic chemical reagent, it is still necessary to pay attention to safe use. Avoid direct contact with skin, eyes and inhalation during operation. The working environment requires good ventilation and the use of personal protective equipment, such as laboratory gloves, eye protection, etc. If swallowed or taken by mistake, seek medical attention immediately.
Last Update：2024-04-09 02:00:57
